Canonical Allele Identifier: PA2826449857
Gene: TYMP HGNC NCBI

Linked Data

ClinVar Variation Id: 2057817
ClinVar RCV Id: RCV002942090
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244918.1:p.Ile71Met
CA10321852
NM_001257989.1:c.213C>G