Allele Registry

Canonical Allele Identifier: PA645390055

Gene: PTS HGNC NCBI

ClinVar RCV:

RCV000413378

RCV001261646

ClinVar Variation:

372484

HGVS (amino-acid)	Matching Registered Transcripts
NP_000308.1:p.Met80Val	CA16042813 NM_000317.3:c.238A>G