TLN2 c.7141C>G ;(p.P2381A)

Variant ID: 15-63127948-C-G

NM_015059.2(TLN2):c.7141C>G;(p.P2381A)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


The Cardiac Genome Clinic: implementing genome sequencing in pediatric heart disease.

Genetics In Medicine : Official Journal Of The American College Of Medical Genetics
Reuter, Miriam S MS; Chaturvedi, Rajiv R RR; Liston, Eriskay E; Manshaei, Roozbeh R; Aul, Ritu B RB; Bowdin, Sarah S; Cohn, Iris I; Curtis, Meredith M; Dhir, Priya P; Hayeems, Robin Z RZ; Hosseini, S Mohsen SM; Khan, Reem R; Ly, Linh G LG; Marshall, Christian R CR; Mertens, Luc L; Okello, John B A JBA; Pereira, Sergio L SL; Raajkumar, Akshaya A; Seed, Mike M; Thiruvahindrapuram, Bhooma B; Scherer, Stephen W SW; Kim, Raymond H RH; Jobling, Rebekah K RK
Publication Date: 2020-06

Variant appearance in text: TLN2: Pro2381Ala
PubMed Link: 32037394
Variant Present in the following documents:
  • Main text
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