Canonical Allele Identifier: PA113222
Gene: PTS HGNC NCBI

Linked Data

ClinVar Variation Id: 1303150
ClinVar RCV Id: RCV001756649
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000308.1:p.Phe100Val
CA382627887
NM_000317.3:c.298T>G