Allele Registry

Canonical Allele Identifier: PA916045273

Gene: SCN9A HGNC NCBI

Linked Data - NCBI & NCI

ClinVar Allele:

167458

ClinVar RCV:

RCV000144932

RCV000218739

RCV000281545

RCV000284837

RCV000398464

RCV000416064

RCV000986925

RCV001083229

RCV001094589

RCV002415629

RCV004532638

ClinVar Variation:

157597

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001352465.1:p.Ile750Val	CA171007 NM_001365536.1:c.2248A>G