Allele Registry

Canonical Allele Identifier: PA126808

Gene: TYMP HGNC NCBI

ClinVar RCV:

RCV000018146

RCV003330395

RCV003556042

ClinVar Variation:

16666

HGVS (amino-acid)	Matching Registered Transcripts
NP_001244918.1:p.Leu285Pro	CA126803 NM_001257989.1:c.854T>C