Canonical Allele Identifier: PA2825568000
Gene: TYMP HGNC NCBI

Linked Data

ClinVar Variation Id: 223051
ClinVar RCV Id: RCV000208689

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107227.1:p.Leu356Pro
CA16616793
NM_001113755.3:c.1067T>C