Canonical Allele Identifier: PA2826449388
Gene: TYMP HGNC NCBI

Linked Data

ClinVar Variation Id: 3065101
ClinVar RCV Id: RCV003990178

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244917.1:p.Gly119Glu
CA325565272
NM_001257988.1:c.356G>A