Allele Registry

Canonical Allele Identifier: PA126800

Gene: TYMP HGNC NCBI

ClinVar RCV:

RCV000018145

RCV003228895

ClinVar Variation:

16665

HGVS (amino-acid)	Matching Registered Transcripts
NP_001107227.1:p.Arg202Thr	CA126797 NM_001113755.3:c.605G>C