Allele Registry

Canonical Allele Identifier: PA2826449652

Gene: TYMP HGNC NCBI

ClinVar RCV:

RCV000208644

ClinVar Variation:

223053

HGVS (amino-acid)	Matching Registered Transcripts
NP_001244917.1:p.Gly387Ser	CA16616795 NM_001257988.1:c.1159G>A