Allele Registry

Canonical Allele Identifier: PA2825567834

Gene: TYMP HGNC NCBI

ClinVar RCV:

RCV000208663

ClinVar Variation:

223036

HGVS (amino-acid)	Matching Registered Transcripts
NP_001107227.1:p.Val208Gly	CA16616783 NM_001113755.3:c.623T>G