Canonical Allele Identifier: PA2499243178
Gene: TYMP HGNC NCBI

Linked Data

ClinVar Variation Id: 1148363
ClinVar RCV Id: RCV001488218
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244918.1:p.Pro390Ser
CA412197168
NM_001257989.1:c.1168C>T