Canonical Allele Identifier: PA2827923051
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 9401

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341630.1:p.Asp1274Asn
CA017530
NM_001354701.2:c.3820G>A