Allele Registry

Canonical Allele Identifier: PA319170

Gene: TPP1 HGNC NCBI

ClinVar Allele:

202589

ClinVar RCV:

RCV000189761

RCV001833128

ClinVar Variation:

207571

HGVS (amino-acid)	Matching Registered Transcripts
NP_000382.3:p.Val142Gly	CA319169 NM_000391.4:c.425T>G