Allele Registry

Canonical Allele Identifier: PA100817

Gene: TYMP HGNC NCBI

ClinVar RCV:

RCV000018141

RCV002513094

ClinVar Variation:

16661

HGVS (amino-acid)	Matching Registered Transcripts
NP_001107227.1:p.Arg44Gln	CA126779 NM_001113755.3:c.131G>A