Canonical Allele Identifier: PA2825941461
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 9400

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Glu1053Lys
CA016871
NM_001160160.2:c.3157G>A