Allele Registry

Canonical Allele Identifier: PA645400131

Gene: TYMP HGNC NCBI

ClinVar RCV:

RCV000208625

RCV002515560

ClinVar Variation:

223055

HGVS (amino-acid)	Matching Registered Transcripts
NP_001244918.1:p.Gly433Ser	CA16616797 NM_001257989.1:c.1297G>A