Allele Registry

Canonical Allele Identifier: PA181453

Gene: SCN5A HGNC NCBI

Linked Data - NCBI & NCI

ClinVar Allele:

78916

ClinVar RCV:

RCV000058824

RCV000154829

RCV000242689

RCV000678920

RCV001149898

RCV001149899

RCV001149900

RCV001149901

RCV001149902

RCV001842403

RCV003149714

RCV004542729

ClinVar Variation:

68024

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000326.2:p.Pro2005Ala	CA019597 NM_000335.5:c.6013C>G