Canonical Allele Identifier: PA2580252974
Gene: TYMP HGNC NCBI

Linked Data

ClinVar Variation Id: 2139320
ClinVar RCV Id: RCV003050953

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001944.1:p.Cys280Arg
CA412199164
NM_001953.5:c.838T>C