Allele Registry

Canonical Allele Identifier: PA103007

Gene: GRN HGNC NCBI

ClinVar Allele:

31052

ClinVar RCV:

RCV000017386

RCV000084421

RCV001851887

ClinVar Variation:

16013

HGVS (amino-acid)	Matching Registered Transcripts
NP_002078.1:p.Ala9Asp	CA225199 NM_002087.4:c.26C>A