Canonical Allele Identifier: PA2827923846
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 9375

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341630.1:p.Tyr1776Cys
CA019196
NM_001354701.2:c.5327A>G