Allele Registry

Canonical Allele Identifier: PA099719

Gene: SLC22A12 HGNC NCBI

ClinVar RCV:

RCV000003692

ClinVar Variation:

3515

HGVS (amino-acid)	Matching Registered Transcripts
NP_653186.2:p.Leu418Arg	CA116316 NM_144585.4:c.1253T>G