Allele Registry

Canonical Allele Identifier: PA2828180179

Gene: SCN9A HGNC NCBI

ClinVar RCV:

RCV000006737

ClinVar Variation:

6365

HGVS (amino-acid)	Matching Registered Transcripts
NP_001352465.1:p.Phe216Ser	CA340557 NM_001365536.1:c.647T>C