Allele Registry

Canonical Allele Identifier: PA2825568585

Gene: TYMP HGNC NCBI

ClinVar RCV:

RCV000208644

ClinVar Variation:

223053

HGVS (amino-acid)	Matching Registered Transcripts
NP_001107228.1:p.Gly387Ser	CA16616795 NM_001113756.3:c.1159G>A