Allele Registry

Canonical Allele Identifier: PA2828088073

Gene: SLC29A3 HGNC NCBI

ClinVar Allele:

15608

ClinVar RCV:

RCV000000599

RCV003398400

ClinVar Variation:

569

HGVS (amino-acid)	Matching Registered Transcripts
NP_001350447.1:p.Thr371Arg	CA114354 NM_001363518.2:c.1112C>G