Canonical Allele Identifier: PA2825941609
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67796

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Glu1137Ala
CA017144
NM_001160160.2:c.3410A>C