Allele Registry

Canonical Allele Identifier: PA915977615

Gene: TYMP HGNC NCBI

ClinVar RCV:

RCV000018145

RCV003228895

ClinVar Variation:

16665

HGVS (amino-acid)	Matching Registered Transcripts
NP_001944.1:p.Arg202Thr	CA126797 NM_001953.5:c.605G>C