Canonical Allele Identifier: PA2580268962
Gene: GRN HGNC NCBI

Linked Data

ClinVar Variation Id: 2187565
ClinVar RCV Id: RCV002615860
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002078.1:p.Gly333Val
CA399765231
NM_002087.4:c.998G>T