Canonical Allele Identifier: PA2826449917
Gene: TYMP HGNC NCBI

Linked Data

ClinVar Variation Id: 3185244
ClinVar RCV Id: RCV004484095
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244918.1:p.Gly137Val
CA412201916
NM_001257989.1:c.410G>T