Canonical Allele Identifier: PA2825774378
Gene: GFAP HGNC NCBI

Linked Data

ClinVar Variation Id: 2119962
ClinVar RCV Id: RCV003024914

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124491.1:p.Ala96Pro
CA399848479
NM_001131019.3:c.286G>C