Canonical Allele Identifier: PA2825567912
Gene: TYMP HGNC NCBI

Linked Data

ClinVar Variation Id: 223041

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107227.1:p.His283Asp
CA16616787
NM_001113755.3:c.847C>G