Allele Registry

Canonical Allele Identifier: PA2826450071

Gene: TYMP HGNC NCBI

ClinVar RCV:

RCV000208708

ClinVar Variation:

223049

HGVS (amino-acid)	Matching Registered Transcripts
NP_001244918.1:p.Gly311Cys	CA16616791 NM_001257989.1:c.931G>T