SCN5A c.1949_1951del ;(p.V650del)

Variant ID: 3-38640480-TCTA-T

NM_000335.4(SCN5A):c.1949_1951del;(p.V650del)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Childhood onset nexilin dilated cardiomyopathy: A heterozygous and a homozygous case.

American Journal Of Medical Genetics. Part A
Bruyndonckx, Luc L; Vogelzang, Judith L JL; Bugiani, Marianna M; Straver, Bart B; Kuipers, Irene M IM; Onland, Wes W; Nannenberg, Eline A EA; Clur, Sally-Ann SA; van der Crabben, Saskia N SN
Publication Date: 2021-08

Variant appearance in text: SCN5A: 1949_1951del
PubMed Link: 33949776
Variant Present in the following documents:
  • Main text
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