Allele Registry

Canonical Allele Identifier: PA2826449754

Gene: TYMP HGNC NCBI

ClinVar RCV:

RCV000208631

ClinVar Variation:

223087

HGVS (amino-acid)	Matching Registered Transcripts
NP_001244917.1:p.Pro466_Phe467del	CA16616819 NM_001257988.1:c.1395_1400del