Canonical Allele Identifier: PA2741889416
Gene: GRN HGNC NCBI

Linked Data

ClinVar Variation Id: 2940195
ClinVar RCV Id: RCV003797553

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002078.1:p.Pro405Ser
CA290926640
NM_002087.4:c.1213C>T