Canonical Allele Identifier: PA2825497354
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1000020

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Glu1858Val
CA352140568
NM_001099405.2:c.5573A>T