Allele Registry

Canonical Allele Identifier: PA2828077382

Gene: SLC52A2 HGNC NCBI

ClinVar RCV:

RCV000082865

ClinVar Variation:

96703

HGVS (amino-acid)	Matching Registered Transcripts
NP_001350051.1:p.Tyr141Cys	CA345438 NM_001363122.2:c.422A>G