Canonical Allele Identifier: PA2825132619
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1330809

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Lys1885Thr
CA352140442
NM_000335.5:c.5654A>C