Canonical Allele Identifier: PA2825945133
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67904

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153633.1:p.Leu1447Val
CA018357
NM_001160161.2:c.4339C>G