Allele Registry

Canonical Allele Identifier: PA2826449495

Gene: TYMP HGNC NCBI

ClinVar RCV:

RCV000208703

ClinVar Variation:

223040

HGVS (amino-acid)	Matching Registered Transcripts
NP_001244917.1:p.Thr254Pro	CA16616786 NM_001257988.1:c.760A>C