Canonical Allele Identifier: PA113139
Gene: PTS HGNC NCBI
ClinVar RCV:
RCV000000511
ClinVar Variation:
482
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000308.1:p.Asn47Asp
CA114321
NM_000317.3:c.139A>G