Canonical Allele Identifier: PA2825128828
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 578662

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Gly298Asp
CA065869
NM_000335.5:c.893G>A