Canonical Allele Identifier: PA2825567688
Gene: TYMP HGNC NCBI

Linked Data

ClinVar Variation Id: 223017
ClinVar RCV Id: RCV000208699
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107227.1:p.Leu49Arg
CA16616770
NM_001113755.3:c.146T>G