Canonical Allele Identifier: PA915959897
Gene: PTS HGNC NCBI

Linked Data

ClinVar Variation Id: 663940
ClinVar RCV Id: RCV000821922
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000308.1:p.His51Tyr
CA6278478
NM_000317.3:c.151C>T