Canonical Allele Identifier: PA291568
Gene: TYMP HGNC NCBI

Linked Data

ClinVar Variation Id: 137872
ClinVar RCV Id: RCV000126198 RCV000513951 RCV001145864 RCV003925249
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244918.1:p.Arg81Gln
CA291564
NM_001257989.1:c.242G>A