Canonical Allele Identifier: PA2825568652
Gene: TYMP HGNC NCBI

Linked Data

ClinVar Variation Id: 223055

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107228.1:p.Gly428Ser
CA16616797
NM_001113756.3:c.1282G>A