Allele Registry

Canonical Allele Identifier: PA345437

Gene: SLC52A2 HGNC NCBI

ClinVar Allele:

102593

ClinVar RCV:

RCV000082864

ClinVar Variation:

96702

HGVS (amino-acid)	Matching Registered Transcripts
NP_078807.1:p.Ala284Asp	CA345434 NM_024531.5:c.851C>A