Canonical Allele Identifier: PA2829356621
Gene: GRN HGNC NCBI

Linked Data

ClinVar Variation Id: 3102718
ClinVar RCV Id: RCV004396108
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002078.1:p.Gly443Ser
CA8602171
NM_002087.4:c.1327G>A