Canonical Allele Identifier: PA2580269029
Gene: GRN HGNC NCBI

Linked Data

ClinVar Variation Id: 2162242
ClinVar RCV Id: RCV003091181

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002078.1:p.Ser449Arg
CA399769097
NM_002087.4:c.1345A>C
CA399769119
NM_002087.4:c.1347C>G
CA399769124
NM_002087.4:c.1347C>A