Canonical Allele Identifier: PA2825128169
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 936508

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Thr38Ile
CA352158800
NM_000335.5:c.113C>T