Canonical Allele Identifier: PA645400116
Gene: TYMP HGNC NCBI

Linked Data

ClinVar Variation Id: 223064
ClinVar RCV Id: RCV000208629 RCV000606736 RCV001255087
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244918.1:p.Gly392Ser
CA16616801
NM_001257989.1:c.1174G>A