Allele Registry

Canonical Allele Identifier: PA1139742823

Gene: SCN9A HGNC NCBI

ClinVar RCV:

RCV001061174

ClinVar Variation:

855831

HGVS (amino-acid)	Matching Registered Transcripts
NP_001352465.1:p.Ala874Ser	CA1944233 NM_001365536.1:c.2620G>T