Allele Registry

Canonical Allele Identifier: PA2828180140

Gene: SCN9A HGNC NCBI

ClinVar RCV:

RCV000144930

RCV000144931

RCV000178871

RCV000331310

RCV000382273

RCV000421273

RCV001081785

ClinVar Variation:

157596

HGVS (amino-acid)	Matching Registered Transcripts
NP_001352465.1:p.Arg185His	CA171004 NM_001365536.1:c.554G>A