Allele Registry

Canonical Allele Identifier: PA2825567877

Gene: TYMP HGNC NCBI

ClinVar RCV:

RCV000208703

ClinVar Variation:

223040

HGVS (amino-acid)	Matching Registered Transcripts
NP_001107227.1:p.Thr254Pro	CA16616786 NM_001113755.3:c.760A>C