Canonical Allele Identifier: PA2825568244
Gene: TYMP HGNC NCBI

Linked Data

ClinVar Variation Id: 215327

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107228.1:p.Gly64Arg
CA324437
NM_001113756.3:c.190G>A
CA412202503
NM_001113756.3:c.190G>C