Allele Registry

Canonical Allele Identifier: PA2826449342

Gene: TYMP HGNC NCBI

ClinVar RCV:

RCV000336790

ClinVar Variation:

342155

HGVS (amino-acid)	Matching Registered Transcripts
NP_001244917.1:p.Gly68Ser	CA10321854 NM_001257988.1:c.202G>A