Allele Registry

Canonical Allele Identifier: PA2499299307

Gene: SLC22A1 HGNC NCBI

ClinVar RCV:

RCV001691749

ClinVar Variation:

1283709

HGVS (amino-acid)	Matching Registered Transcripts
NP_694857.1:p.Met408Val	CA4084017 NM_153187.2:c.1222A>G