Canonical Allele Identifier: PA2825568258
Gene: TYMP HGNC NCBI

Linked Data

ClinVar Variation Id: 448846
ClinVar RCV Id: RCV000518152

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107228.1:p.Met74Lys
CA412202370
NM_001113756.3:c.221T>A