Allele Registry

Canonical Allele Identifier: PA916045244

Gene: SCN9A HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000006739

RCV000153918

RCV000415152

RCV000488281

RCV001083774

RCV001133028

RCV001133029

RCV001133030

RCV002415403

RCV004532301

ClinVar Variation:

6367

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001352465.1:p.Lys666Arg	CA118167 NM_001365536.1:c.1997A>G