Canonical Allele Identifier: PA2573166206
Gene: PTS HGNC NCBI

Linked Data

ClinVar Variation Id: 1508903
ClinVar RCV Id: RCV002016446

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000308.1:p.Tyr53Ser
CA382627124
NM_000317.3:c.158A>C