Allele Registry

Canonical Allele Identifier: PA2828180188

Gene: SCN9A HGNC NCBI

Linked Data - NCBI & NCI

ClinVar Allele:

195314

ClinVar RCV:

RCV000179414

RCV000192901

RCV000515449

RCV000540917

RCV001133337

RCV001133338

RCV001133339

RCV001195747

RCV002362922

ClinVar Variation:

198153

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001352465.1:p.Ile228Met	CA206037 NM_001365536.1:c.684C>G