Canonical Allele Identifier: PA113149
Gene: PTS HGNC NCBI

Linked Data

ClinVar Variation Id: 479
ClinVar RCV Id: RCV000000508 RCV003156211 RCV003924789
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000308.1:p.Asn52Ser
CA114318
NM_000317.3:c.155A>G