Allele Registry

Canonical Allele Identifier: PA181494

Gene: SCN5A HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000154839

RCV000729899

RCV000852964

RCV001145076

RCV001145077

RCV001147026

RCV001147027

RCV001147028

RCV001147029

RCV001842482

RCV002321640

ClinVar Variation:

178130

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001092874.1:p.Ala1088Thr	CA016979 NM_001099404.2:c.3262G>A