Canonical Allele Identifier: PA2825493923
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 201466

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Ala647Ser
CA015591
NM_001099405.2:c.1939G>T