Allele Registry

Canonical Allele Identifier: PA099678

Gene: SLC22A12 HGNC NCBI

ClinVar RCV:

RCV000348762

RCV003409469

RCV003546509

RCV003993926

ClinVar Variation:

305239

HGVS (amino-acid)	Matching Registered Transcripts
NP_653186.2:p.Gln382Leu	CA6077325 NM_144585.4:c.1145A>T