Allele Registry

Canonical Allele Identifier: PA2826449714

Gene: TYMP HGNC NCBI

ClinVar RCV:

RCV000208625

RCV002515560

ClinVar Variation:

223055

HGVS (amino-acid)	Matching Registered Transcripts
NP_001244917.1:p.Gly428Ser	CA16616797 NM_001257988.1:c.1282G>A