Allele Registry

Canonical Allele Identifier: PA2825567861

Gene: TYMP HGNC NCBI

ClinVar RCV:

RCV000208661

ClinVar Variation:

223039

HGVS (amino-acid)	Matching Registered Transcripts
NP_001107227.1:p.Ala239Thr	CA16616785 NM_001113755.3:c.715G>A