Canonical Allele Identifier: PA2826449878
Gene: TYMP HGNC NCBI

Linked Data

ClinVar Variation Id: 1691348
ClinVar RCV Id: RCV002254446
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244918.1:p.Gln93Leu
CA412202190
NM_001257989.1:c.278A>T