Allele Registry

Canonical Allele Identifier: PA2828088057

Gene: SLC29A3 HGNC NCBI

ClinVar RCV:

RCV000000593

RCV002272004

ClinVar Variation:

563

HGVS (amino-acid)	Matching Registered Transcripts
NP_001350447.1:p.Gly349Ser	CA114349 NM_001363518.2:c.1045G>A