Canonical Allele Identifier: PA307392
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 201474

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Arg811Cys
CA016138
NM_001099404.2:c.2431C>T