Allele Registry

Canonical Allele Identifier: PA2825568494

Gene: TYMP HGNC NCBI

ClinVar RCV:

RCV000208708

ClinVar Variation:

223049

HGVS (amino-acid)	Matching Registered Transcripts
NP_001107228.1:p.Gly311Cys	CA16616791 NM_001113756.3:c.931G>T