Canonical Allele Identifier: PA658678326
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 463317

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Ala993Thr
CA061107
NM_198056.3:c.2977G>A