Allele Registry

Canonical Allele Identifier: PA2825567948

Gene: TYMP HGNC NCBI

ClinVar RCV:

RCV000208708

ClinVar Variation:

223049

HGVS (amino-acid)	Matching Registered Transcripts
NP_001107227.1:p.Gly311Cys	CA16616791 NM_001113755.3:c.931G>T