Canonical Allele Identifier: PA2826450036
Gene: TYMP HGNC NCBI

Linked Data

ClinVar Variation Id: 1921794
ClinVar RCV Id: RCV002613301
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244918.1:p.Val281Met
CA412199142
NM_001257989.1:c.841G>A