Canonical Allele Identifier: PA645407212
Gene: TYMP HGNC NCBI

Linked Data

ClinVar Variation Id: 223032
ClinVar RCV Id: RCV000208713

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001944.1:p.Leu177Pro
CA16616782
NM_001953.5:c.530T>C