Allele Registry

Canonical Allele Identifier: PA103399

Gene: SLC29A3 HGNC NCBI

ClinVar RCV:

RCV000000595

RCV000414664

ClinVar Variation:

565

HGVS (amino-acid)	Matching Registered Transcripts
NP_060814.4:p.Gly437Arg	CA114352 NM_018344.6:c.1309G>A CA377117232 NM_018344.6:c.1309G>C