Canonical Allele Identifier: PA2827923601
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67940

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341630.1:p.Gly1623Glu
CA018747
NM_001354701.2:c.4868G>A