Allele Registry

Canonical Allele Identifier: PA916045380

Gene: SCN9A HGNC NCBI

Linked Data - NCBI & NCI

ClinVar Allele:

135712

ClinVar RCV:

RCV000176065

RCV000328939

RCV000335798

RCV000383539

RCV000389147

RCV000422016

RCV000714847

RCV000714848

RCV000768312

RCV001080021

RCV002345422

RCV003224155

ClinVar Variation:

130265

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001352465.1:p.Asn1256Ser	CA201784 NM_001365536.1:c.3767A>G