Allele Registry

Canonical Allele Identifier: PA2825568220

Gene: TYMP HGNC NCBI

ClinVar RCV:

RCV000018141

RCV002513094

ClinVar Variation:

16661

HGVS (amino-acid)	Matching Registered Transcripts
NP_001107228.1:p.Arg44Gln	CA126779 NM_001113756.3:c.131G>A