Allele Registry

Canonical Allele Identifier: PA2825567757

Gene: TYMP HGNC NCBI

ClinVar RCV:

RCV000208638

ClinVar Variation:

223024

HGVS (amino-acid)	Matching Registered Transcripts
NP_001107227.1:p.Asp114Asn	CA16616776 NM_001113755.3:c.340G>A