Allele Registry

Canonical Allele Identifier: PA103387

Gene: SLC29A3 HGNC NCBI

ClinVar RCV:

RCV000000593

RCV002272004

ClinVar Variation:

563

HGVS (amino-acid)	Matching Registered Transcripts
NP_060814.4:p.Gly427Ser	CA114349 NM_018344.6:c.1279G>A