Canonical Allele Identifier: PA2580181596
Gene: TYMP HGNC NCBI

Linked Data

ClinVar Variation Id: 1934350
ClinVar RCV Id: RCV002631881
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244918.1:p.Ala387Gly
CA412197194
NM_001257989.1:c.1160C>G