Canonical Allele Identifier: PA2827921481
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 633409
ClinVar RCV Id: RCV000781838

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341630.1:p.Ala204Thr
CA352153406
NM_001354701.2:c.610G>A