Canonical Allele Identifier: PA2829364527
Gene: TYMP HGNC NCBI

Linked Data

ClinVar Variation Id: 223055
ClinVar RCV Id: RCV000208625 RCV002515560
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001944.1:p.Gly428Ser
CA16616797
NM_001953.5:c.1282G>A