Allele Registry

Canonical Allele Identifier: PA126795

Gene: TYMP HGNC NCBI

ClinVar RCV:

RCV000018144

ClinVar Variation:

16664

HGVS (amino-acid)	Matching Registered Transcripts
NP_001244917.1:p.Gly311Arg	CA126791 NM_001257988.1:c.931G>C