Canonical Allele Identifier: PA658663351
Gene: TYMP HGNC NCBI

Linked Data

ClinVar Variation Id: 448846
ClinVar RCV Id: RCV000518152
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244918.1:p.Met74Lys
CA412202370
NM_001257989.1:c.221T>A