Allele Registry

Canonical Allele Identifier: PA291598

Gene: TYMP HGNC NCBI

ClinVar RCV:

RCV000126205

RCV000306032

RCV000373441

RCV000676457

RCV001274280

RCV003975113

ClinVar Variation:

137878

HGVS (amino-acid)	Matching Registered Transcripts
NP_001244917.1:p.Ala465Thr	CA291595 NM_001257988.1:c.1393G>A