Canonical Allele Identifier: PA2573223687
Gene: GRN HGNC NCBI

Linked Data

ClinVar Variation Id: 1525789
ClinVar RCV Id: RCV002036950
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002078.1:p.Thr382Met
CA8602108
NM_002087.4:c.1145C>T