Allele Registry

Canonical Allele Identifier: PA916045304

Gene: SCN9A HGNC NCBI

ClinVar RCV:

RCV000020513

ClinVar Variation:

21346

HGVS (amino-acid)	Matching Registered Transcripts
NP_001352465.1:p.Ala874Pro	CA341936 NM_001365536.1:c.2620G>C