Canonical Allele Identifier: PA2825940783
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 949946
ClinVar RCV Id: RCV003541296

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Val595Ala
CA352146173
NM_001160160.2:c.1784T>C