Allele Registry

Canonical Allele Identifier: PA126787

Gene: TYMP HGNC NCBI

ClinVar RCV:

RCV000018143

RCV000199543

ClinVar Variation:

16663

HGVS (amino-acid)	Matching Registered Transcripts
NP_001107227.1:p.Val208Met	CA126784 NM_001113755.3:c.622G>A