Canonical Allele Identifier: PA1139722926
Gene: TYMP HGNC NCBI

Linked Data

ClinVar Variation Id: 902222

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001944.1:p.Ser65Gly
CA10321860
NM_001953.5:c.193A>G