Canonical Allele Identifier: PA2826449729
Gene: TYMP HGNC NCBI

Linked Data

ClinVar Variation Id: 2418087
ClinVar RCV Id: RCV003118196

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244917.1:p.Arg442Trp
CA412196452
NM_001257988.1:c.1324C>T