Allele Registry

Canonical Allele Identifier: PA126782

Gene: TYMP HGNC NCBI

ClinVar RCV:

RCV000018141

RCV002513094

ClinVar Variation:

16661

HGVS (amino-acid)	Matching Registered Transcripts
NP_001244917.1:p.Arg44Gln	CA126779 NM_001257988.1:c.131G>A