Canonical Allele Identifier: PA2580181612
Gene: TYMP HGNC NCBI

Linked Data

ClinVar Variation Id: 2418087
ClinVar RCV Id: RCV003118196

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244918.1:p.Arg447Trp
CA412196452
NM_001257989.1:c.1339C>T