Canonical Allele Identifier: PA2825941705
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1172206

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Glu1202Ala
CA352138102
NM_001160160.2:c.3605A>C