Canonical Allele Identifier: PA2825568120
Gene: TYMP HGNC NCBI

Linked Data

ClinVar Variation Id: 1432203
ClinVar RCV Id: RCV001981956

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107227.1:p.Arg442Gln
CA412196449
NM_001113755.3:c.1325G>A