Allele Registry

Canonical Allele Identifier: PA916045505

Gene: SCN9A HGNC NCBI

ClinVar RCV:

RCV000467475

ClinVar Variation:

408574

HGVS (amino-acid)	Matching Registered Transcripts
NP_001352465.1:p.Asp1959Ala	CA16610170 NM_001365536.1:c.5876A>C