Allele Registry

Canonical Allele Identifier: PA108679

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_932173.1:p.Val1951Leu	CA019509 NM_198056.3:c.5851G>T CA352139705 NM_198056.3:c.5851G>C