Canonical Allele Identifier: PA103007
Gene: GRN HGNC NCBI

Linked Data

ClinVar Variation Id: 16013

Amino-acid Alleles

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