Allele Registry

Canonical Allele Identifier: PA645400118

Gene: TYMP HGNC NCBI

ClinVar RCV:

RCV000208687

RCV003235134

ClinVar Variation:

223054

HGVS (amino-acid)	Matching Registered Transcripts
NP_001244918.1:p.Gly392Asp	CA16616796 NM_001257989.1:c.1175G>A