Allele Registry

Canonical Allele Identifier: PA099669

Gene: SLC22A12 HGNC NCBI

ClinVar Allele:

18555

ClinVar RCV:

RCV000003693

RCV000826151

RCV002512717

ClinVar Variation:

3516

HGVS (amino-acid)	Matching Registered Transcripts
NP_653186.2:p.Arg90His	CA116317 NM_144585.4:c.269G>A