Canonical Allele Identifier: PA2826449727
Gene: TYMP HGNC NCBI

Linked Data

ClinVar Variation Id: 1432203
ClinVar RCV Id: RCV001981956

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244917.1:p.Arg442Gln
CA412196449
NM_001257988.1:c.1325G>A