Allele Registry

Canonical Allele Identifier: PA2826449651

Gene: TYMP HGNC NCBI

ClinVar RCV:

RCV000208687

RCV003235134

ClinVar Variation:

223054

HGVS (amino-acid)	Matching Registered Transcripts
NP_001244917.1:p.Gly387Asp	CA16616796 NM_001257988.1:c.1160G>A