Allele Registry

Canonical Allele Identifier: PA2826554256

Gene: SLC22A12 HGNC NCBI

ClinVar RCV:

RCV000003692

ClinVar Variation:

3515

HGVS (amino-acid)	Matching Registered Transcripts
NP_001263256.1:p.Leu310Arg	CA116316 NM_001276327.2:c.929T>G