Allele Registry

Canonical Allele Identifier: PA2828180376

Gene: SCN9A HGNC NCBI

ClinVar RCV:

RCV000221632

RCV000692363

RCV000765528

RCV001336519

RCV002381753

ClinVar Variation:

234638

HGVS (amino-acid)	Matching Registered Transcripts
NP_001352465.1:p.Leu427Ser	CA1944557 NM_001365536.1:c.1280T>C