Allele Registry

Canonical Allele Identifier: PA645400144

Gene: TYMP HGNC NCBI

ClinVar RCV:

RCV000208631

ClinVar Variation:

223087

HGVS (amino-acid)	Matching Registered Transcripts
NP_001244918.1:p.Pro471_Phe472del	CA16616819 NM_001257989.1:c.1410_1415del