Allele Registry

Canonical Allele Identifier: PA645390070

Gene: PTS HGNC NCBI

ClinVar RCV:

RCV000413988

RCV001206459

ClinVar Variation:

372485

HGVS (amino-acid)	Matching Registered Transcripts
NP_000308.1:p.Asp94Gly	CA16042731 NM_000317.3:c.281A>G