Canonical Allele Identifier: PA2825568538
Gene: TYMP HGNC NCBI

Linked Data

ClinVar Variation Id: 2138462

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107228.1:p.Leu347Pro
CA412197822
NM_001113756.3:c.1040T>C