Canonical Allele Identifier: PA2825538084
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1026458
ClinVar RCV Id: RCV003656875

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Gly605Ala
CA352146049
NM_001099404.2:c.1814G>C