Allele Registry

Canonical Allele Identifier: PA645407241

Gene: TYMP HGNC NCBI

ClinVar RCV:

RCV000208661

ClinVar Variation:

223039

HGVS (amino-acid)	Matching Registered Transcripts
NP_001944.1:p.Ala239Thr	CA16616785 NM_001953.5:c.715G>A