Canonical Allele Identifier: PA2825942109
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1699580
ClinVar RCV Id: RCV002273437

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Leu1461Pro
CA352145319
NM_001160160.2:c.4382T>C