Allele Registry

Canonical Allele Identifier: PA2828180575

Gene: SCN9A HGNC NCBI

ClinVar RCV:

RCV000023303

RCV002513185

ClinVar Variation:

30358

HGVS (amino-acid)	Matching Registered Transcripts
NP_001352465.1:p.Asp623Asn	CA129152 NM_001365536.1:c.1867G>A