Allele Registry

Canonical Allele Identifier: PA111746

Gene: SLC19A2 HGNC NCBI

ClinVar RCV:

RCV000006321

RCV000486790

ClinVar Variation:

5957

HGVS (amino-acid)	Matching Registered Transcripts
NP_008927.1:p.Gly172Asp	CA253658 NM_006996.3:c.515G>A