Allele Registry

Canonical Allele Identifier: PA2826449561

Gene: TYMP HGNC NCBI

ClinVar RCV:

RCV000208664

RCV001853327

ClinVar Variation:

223048

HGVS (amino-acid)	Matching Registered Transcripts
NP_001244917.1:p.Gly311Ser	CA10321513 NM_001257988.1:c.931G>A