Canonical Allele Identifier: PA320186
Gene: TYMP HGNC NCBI

Linked Data

ClinVar Variation Id: 215342
ClinVar RCV Id: RCV001260913 RCV002517272
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244917.1:p.Pro131Thr
CA320183
NM_001257988.1:c.391C>A