Canonical Allele Identifier: PA2826449892
Gene: TYMP HGNC NCBI

Linked Data

ClinVar Variation Id: 1163691
ClinVar RCV Id: RCV001508951

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244918.1:p.Gln110His
CA412202073
NM_001257989.1:c.330G>T
CA412202074
NM_001257989.1:c.330G>C