Canonical Allele Identifier: PA2826449801
Gene: TYMP HGNC NCBI

Linked Data

ClinVar Variation Id: 2295049
ClinVar RCV Id: RCV002865032
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244918.1:p.Ser19Phe
CA412203014
NM_001257989.1:c.56C>T