Canonical Allele Identifier: PA915977534
Gene: TYMP HGNC NCBI

Linked Data

ClinVar Variation Id: 191172

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001944.1:p.Gly119Arg
CA236178
NM_001953.5:c.355G>A
CA412202021
NM_001953.5:c.355G>C