Allele Registry

Canonical Allele Identifier: PA2825568558

Gene: TYMP HGNC NCBI

ClinVar RCV:

RCV000199261

RCV001833159

ClinVar Variation:

215338

HGVS (amino-acid)	Matching Registered Transcripts
NP_001107228.1:p.Gly363Arg	CA323791 NM_001113756.3:c.1087G>A CA412197593 NM_001113756.3:c.1087G>C