Allele Registry

Canonical Allele Identifier: PA916045357

Gene: SCN9A HGNC NCBI

ClinVar Allele:

283308

ClinVar RCV:

RCV000298492

RCV000313804

RCV000393826

RCV000393834

RCV001861135

ClinVar Variation:

331971

HGVS (amino-acid)	Matching Registered Transcripts
NP_001352465.1:p.Ser1123Asn	CA1944075 NM_001365536.1:c.3368G>A