Canonical Allele Identifier: PA2741889356
Gene: GRN HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002078.1:p.Pro50Leu
CA8601778
NM_002087.4:c.149C>T