Allele Registry

Canonical Allele Identifier: PA126806

Gene: TYMP HGNC NCBI

ClinVar RCV:

RCV000018146

RCV003330395

RCV003556042

ClinVar Variation:

16666

HGVS (amino-acid)	Matching Registered Transcripts
NP_001107227.1:p.Leu285Pro	CA126803 NM_001113755.3:c.854T>C