Canonical Allele Identifier: PA2826449709
Gene: TYMP HGNC NCBI

Linked Data

ClinVar Variation Id: 990766
ClinVar RCV Id: RCV001278857
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244917.1:p.Val425Ile
CA412196778
NM_001257988.1:c.1273G>A