Allele Registry

Canonical Allele Identifier: PA2828076753

Gene: SLC52A2 HGNC NCBI

ClinVar RCV:

RCV000082865

ClinVar Variation:

96703

HGVS (amino-acid)	Matching Registered Transcripts
NP_001350049.1:p.Tyr305Cys	CA345438 NM_001363120.2:c.914A>G