Allele Registry

Canonical Allele Identifier: PA2580288809

Gene: SLC22A13 HGNC NCBI

ClinVar RCV:

RCV004100477

ClinVar Variation:

2246030

HGVS (amino-acid)	Matching Registered Transcripts
NP_004247.2:p.Asp110His	CA352113445 NM_004256.4:c.328G>C