Canonical Allele Identifier: PA2825940789
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 2774477
ClinVar RCV Id: RCV003592359

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Asn598Asp
CA352146143
NM_001160160.2:c.1792A>G