Allele Registry

Canonical Allele Identifier: PA113157

Gene: PTS HGNC NCBI

ClinVar RCV:

RCV000000512

RCV000502112

RCV003230338

ClinVar Variation:

483

HGVS (amino-acid)	Matching Registered Transcripts
NP_000308.1:p.Asp116Gly	CA114322 NM_000317.3:c.347A>G