FLNB c.479A>C ;(p.N160T)

Variant ID: 3-58062959-A-C

NM_001457.3(FLNB):c.479A>C;(p.N160T)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Mutations responsible for Larsen syndrome cluster in the FLNB protein.

Journal Of Medical Genetics
Zhang, D D; Herring, J A JA; Swaney, S S SS; McClendon, T B TB; Gao, X X; Browne, R H RH; Rathjen, K E KE; Johnston, C E CE; Harris, S S; Cain, N M NM; Wise, C A CA
Publication Date: 2006-05

Variant appearance in text: FLNB: N160T
PubMed Link: 16648377
Variant Present in the following documents:
  • Main text
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