Canonical Allele Identifier: PA2827923203
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1013702
ClinVar RCV Id: RCV003770639

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341630.1:p.Thr1366Pro
CA352146994
NM_001354701.2:c.4096A>C