Allele Registry

Canonical Allele Identifier: PA645500463

Gene: INPPL1 HGNC NCBI

ClinVar RCV:

RCV000224467

ClinVar Variation:

235826

HGVS (amino-acid)	Matching Registered Transcripts
NP_001558.3:p.Arg691Trp	CA10581440 NM_001567.4:c.2071C>T