Canonical Allele Identifier: PA113283
Gene: PTS HGNC NCBI
ClinVar RCV:
RCV000000510
ClinVar Variation:
481
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000308.1:p.Val56Met
CA114320
NM_000317.3:c.166G>A