Allele Registry

Canonical Allele Identifier: PA2829418301

Gene: SLC22A1 HGNC NCBI

ClinVar RCV:

RCV001691749

ClinVar Variation:

1283709

HGVS (amino-acid)	Matching Registered Transcripts
NP_003048.1:p.Met408Val	CA4084017 NM_003057.3:c.1222A>G