Canonical Allele Identifier: PA2825944472
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 2913886
ClinVar RCV Id: RCV003735579

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153633.1:p.Glu1025Lys
CA72926247
NM_001160161.2:c.3073G>A