Allele Registry

Canonical Allele Identifier: PA2826449927

Gene: TYMP HGNC NCBI

ClinVar RCV:

RCV000208704

ClinVar Variation:

223029

HGVS (amino-acid)	Matching Registered Transcripts
NP_001244918.1:p.Asp156Gly	CA16616779 NM_001257989.1:c.467A>G