Allele Registry

Canonical Allele Identifier: PA1139719735

Gene: SLC19A2 HGNC NCBI

ClinVar RCV:

RCV001174381

RCV002559674

ClinVar Variation:

917418

HGVS (amino-acid)	Matching Registered Transcripts
NP_008927.1:p.Pro33Gln	CA343112308 NM_006996.3:c.98C>A