Canonical Allele Identifier: PA2825568535
Gene: TYMP HGNC NCBI

Linked Data

ClinVar Variation Id: 872413
ClinVar RCV Id: RCV001092861

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107228.1:p.Arg345Gln
CA412197854
NM_001113756.3:c.1034G>A