Canonical Allele Identifier: PA265373
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67838

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Gly1319Val
CA017654
NM_001099404.2:c.3956G>T