Canonical Allele Identifier: PA2825944905
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 201505

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153633.1:p.Ala1303Val
CA017845
NM_001160161.2:c.3908C>T