Canonical Allele Identifier: PA2741889355
Gene: GRN HGNC NCBI
ClinVar RCV:
RCV003803383
ClinVar Variation:
2943825
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002078.1:p.Trp49Cys
CA399759589
NM_002087.4:c.147G>C
CA399759591
NM_002087.4:c.147G>T