Canonical Allele Identifier: PA2826449337
Gene: TYMP HGNC NCBI

Linked Data

ClinVar Variation Id: 902222

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244917.1:p.Ser65Gly
CA10321860
NM_001257988.1:c.193A>G