Allele Registry

Canonical Allele Identifier: PA2828374797

Gene: SLC52A3 HGNC NCBI

ClinVar Allele:

206629

ClinVar RCV:

RCV000191957

RCV000790977

RCV001589066

RCV002362997

RCV003417696

ClinVar Variation:

210012

HGVS (amino-acid)	Matching Registered Transcripts
NP_001357014.1:p.Asn21Ser	CA346969 NM_001370085.1:c.62A>G