Canonical Allele Identifier: PA2580268969
Gene: GRN HGNC NCBI

Linked Data

ClinVar Variation Id: 2193378
ClinVar RCV Id: RCV002623945

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002078.1:p.Ser353Arg
CA399765581
NM_002087.4:c.1057A>C
CA399765596
NM_002087.4:c.1059C>A
CA399765600
NM_002087.4:c.1059C>G