Allele Registry

Canonical Allele Identifier: PA916045390

Gene: SCN9A HGNC NCBI

ClinVar RCV:

RCV000276112

RCV000340680

RCV000375646

RCV000376885

RCV000412791

RCV000647772

RCV001001973

ClinVar Variation:

331965

HGVS (amino-acid)	Matching Registered Transcripts
NP_001352465.1:p.Ile1315Thr	CA1943972 NM_001365536.1:c.3944T>C