Canonical Allele Identifier: PA2825128094
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 2064744

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Arg14Cys
CA352159424
NM_000335.5:c.40C>T