Canonical Allele Identifier: PA322657
Gene: TYMP HGNC NCBI

Linked Data

ClinVar Variation Id: 215329
ClinVar RCV Id: RCV000198166
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244918.1:p.Gly120Ser
CA322653
NM_001257989.1:c.358G>A