Canonical Allele Identifier: PA2825131262
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 3008823
ClinVar RCV Id: RCV003861950

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Met1334Val
CA72944913
NM_000335.5:c.4000A>G