Allele Registry

Canonical Allele Identifier: PA2825497568

Gene: SCN5A HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000030444

RCV000041632

RCV000058811

RCV000148837

RCV000157493

RCV000171770

RCV000245882

RCV000852961

RCV001145802

RCV001148560

RCV001148561

RCV001148562

RCV001148563

RCV001148564

RCV001841551

RCV003149588

ClinVar Variation:

36765

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001092875.1:p.Val1933Leu	CA019509 NM_001099405.2:c.5797G>T CA352139705 NM_001099405.2:c.5797G>C