Allele Registry

Canonical Allele Identifier: PA2828374792

Gene: SLC52A3 HGNC NCBI

ClinVar RCV:

RCV000191956

ClinVar Variation:

210011

HGVS (amino-acid)	Matching Registered Transcripts
NP_001357014.1:p.Trp17Arg	CA346967 NM_001370085.1:c.49T>C CA407964647 NM_001370085.1:c.49T>A