Canonical Allele Identifier: PA2741891932
Gene: TYMP HGNC NCBI

Linked Data

ClinVar Variation Id: 2901099
ClinVar RCV Id: RCV003731120
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001944.1:p.Pro131Ser
CA412201951
NM_001953.5:c.391C>T