Allele Registry

Canonical Allele Identifier: PA2828180557

Gene: SCN9A HGNC NCBI

ClinVar RCV:

RCV000020511

RCV000118296

RCV000314793

RCV000474864

RCV000713167

RCV001136466

RCV001136467

ClinVar Variation:

21344

HGVS (amino-acid)	Matching Registered Transcripts
NP_001352465.1:p.Pro610Thr	CA155119 NM_001365536.1:c.1828C>A