Allele Registry

Canonical Allele Identifier: PA126761

Gene: TYMP HGNC NCBI

ClinVar RCV:

RCV000018133

RCV000498727

RCV001276276

ClinVar Variation:

16653

HGVS (amino-acid)	Matching Registered Transcripts
NP_001244917.1:p.Glu289Ala	CA126758 NM_001257988.1:c.866A>C