Canonical Allele Identifier: PA1139705623
Gene: GRN HGNC NCBI

Linked Data

ClinVar Variation Id: 864484
ClinVar RCV Id: RCV001071688
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002078.1:p.Thr409Met
CA8602148
NM_002087.4:c.1226C>T