Allele Registry

Canonical Allele Identifier: PA2825568567

Gene: TYMP HGNC NCBI

ClinVar RCV:

RCV000208705

RCV002517411

ClinVar Variation:

223052

HGVS (amino-acid)	Matching Registered Transcripts
NP_001107228.1:p.Leu371Pro	CA16616794 NM_001113756.3:c.1112T>C