Allele Registry

Canonical Allele Identifier: PA2825568478

Gene: TYMP HGNC NCBI

ClinVar RCV:

RCV000208710

RCV001853326

ClinVar Variation:

223046

HGVS (amino-acid)	Matching Registered Transcripts
NP_001107228.1:p.Gly298Asp	CA16616790 NM_001113756.3:c.893G>A