Allele Registry

Canonical Allele Identifier: PA2828076789

Gene: SLC52A2 HGNC NCBI

ClinVar Allele:

458407

ClinVar RCV:

RCV000553303

RCV001449687

RCV001561011

RCV002395455

RCV003945299

ClinVar Variation:

473198

HGVS (amino-acid)	Matching Registered Transcripts
NP_001350049.1:p.Val347Met	CA4938356 NM_001363120.2:c.1039G>A