Canonical Allele Identifier: PA113245
Gene: PTS HGNC NCBI

Linked Data

ClinVar Variation Id: 480
ClinVar RCV Id: RCV000000509 RCV002264906 RCV003153291 RCV003982818
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000308.1:p.Pro87Ser
CA114319
NM_000317.3:c.259C>T