Allele Registry

Canonical Allele Identifier: PA2826450057

Gene: TYMP HGNC NCBI

ClinVar RCV:

RCV000208710

RCV001853326

ClinVar Variation:

223046

HGVS (amino-acid)	Matching Registered Transcripts
NP_001244918.1:p.Gly298Asp	CA16616790 NM_001257989.1:c.893G>A