Allele Registry

Canonical Allele Identifier: PA2826108787

Gene: SLC29A3 HGNC NCBI

ClinVar RCV:

RCV000118382

RCV000306476

RCV000400055

RCV001261569

RCV001640095

RCV001824726

ClinVar Variation:

130344

300363

HGVS (amino-acid)	Matching Registered Transcripts
NP_001167569.1:p.Val239Ile	CA155246 NM_001174098.2:c.715G>A CA10635649 NM_001174098.2:c.714_715delinsCA