Canonical Allele Identifier: PA113118
Gene: PTS HGNC NCBI
ClinVar RCV:
RCV000000505
ClinVar Variation:
476
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000308.1:p.Arg25Gln
CA114316
NM_000317.3:c.74G>A