Canonical Allele Identifier: PA2825496144
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1699580
ClinVar RCV Id: RCV002273437

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Leu1444Pro
CA352145319
NM_001099405.2:c.4331T>C