Allele Registry

Canonical Allele Identifier: PA2828077366

Gene: SLC52A2 HGNC NCBI

ClinVar Allele:

102593

ClinVar RCV:

RCV000082864

ClinVar Variation:

96702

HGVS (amino-acid)	Matching Registered Transcripts
NP_001350051.1:p.Ala120Asp	CA345434 NM_001363122.2:c.359C>A