Canonical Allele Identifier: PA2825130368
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 463317

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Ala993Thr
CA061107
NM_000335.5:c.2977G>A