Canonical Allele Identifier: PA330031
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67843

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Ala1329Pro
CA017704
NM_000335.5:c.3985G>C