Canonical Allele Identifier: PA2573187643
Gene: TYMP HGNC NCBI

Linked Data

ClinVar Variation Id: 1537685
ClinVar RCV Id: RCV002159462
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244918.1:p.Leu389Pro
CA412197176
NM_001257989.1:c.1166T>C