Allele Registry

Canonical Allele Identifier: PA2826449384

Gene: TYMP HGNC NCBI

ClinVar RCV:

RCV000208638

ClinVar Variation:

223024

HGVS (amino-acid)	Matching Registered Transcripts
NP_001244917.1:p.Asp114Asn	CA16616776 NM_001257988.1:c.340G>A