Canonical Allele Identifier: PA2825944843
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1303356
ClinVar RCV Id: RCV001757911

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153633.1:p.Val1268Ala
CA352147649
NM_001160161.2:c.3803T>C