Allele Registry

Canonical Allele Identifier: PA2828180560

Gene: SCN9A HGNC NCBI

ClinVar RCV:

RCV003792655

ClinVar Variation:

2931633

HGVS (amino-acid)	Matching Registered Transcripts
NP_001352465.1:p.Pro610Ala	CA59799460 NM_001365536.1:c.1828C>G