Allele Registry

Canonical Allele Identifier: PA263934

Gene: SLC17A5 HGNC NCBI

ClinVar Allele:

71199

ClinVar RCV:

RCV000049973

ClinVar Variation:

56560

HGVS (amino-acid)	Matching Registered Transcripts
NP_036566.1:p.Gly328Glu	CA263933 NM_012434.5:c.983G>A