Canonical Allele Identifier: PA2827923137
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67843

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341630.1:p.Ala1329Pro
CA017704
NM_001354701.2:c.3985G>C