Allele Registry

Canonical Allele Identifier: PA263922

Gene: SLC17A5 HGNC NCBI

ClinVar RCV:

RCV000049966

ClinVar Variation:

56553

HGVS (amino-acid)	Matching Registered Transcripts
NP_036566.1:p.Gly409Glu	CA263921 NM_012434.5:c.1226G>A