Canonical Allele Identifier: PA1139690221
Gene: TYMP HGNC NCBI

Linked Data

ClinVar Variation Id: 990766
ClinVar RCV Id: RCV001278857

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244918.1:p.Val430Ile
CA412196778
NM_001257989.1:c.1288G>A