Allele Registry

Canonical Allele Identifier: PA2826449832

Gene: TYMP HGNC NCBI

ClinVar Allele:

224742

ClinVar RCV:

RCV000208699

ClinVar Variation:

223017

HGVS (amino-acid)	Matching Registered Transcripts
NP_001244918.1:p.Leu49Arg	CA16616770 NM_001257989.1:c.146T>G