Canonical Allele Identifier: PA265609
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67904

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Leu1500Val
CA018357
NM_000335.5:c.4498C>G