Allele Registry

Canonical Allele Identifier: PA916045379

Gene: SCN9A HGNC NCBI

ClinVar RCV:

RCV000302176

RCV000337267

RCV000391769

RCV000408353

ClinVar Variation:

331968

HGVS (amino-acid)	Matching Registered Transcripts
NP_001352465.1:p.Thr1252Ala	CA10612526 NM_001365536.1:c.3754A>G