Allele Registry

Canonical Allele Identifier: PA2826136537

Gene: GRIP1 HGNC NCBI

ClinVar RCV:

RCV001110213

RCV004032152

ClinVar Variation:

881294

HGVS (amino-acid)	Matching Registered Transcripts
NP_001171545.1:p.Lys31Arg	CA6674750 NM_001178074.2:c.92A>G