Canonical Allele Identifier: PA2825567709
Gene: TYMP HGNC NCBI

Linked Data

ClinVar Variation Id: 902222

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107227.1:p.Ser65Gly
CA10321860
NM_001113755.3:c.193A>G