Allele Registry

Canonical Allele Identifier: PA2825774369

Gene: GFAP HGNC NCBI

ClinVar RCV:

RCV002042292

ClinVar Variation:

1351005

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124491.1:p.Val87Phe	CA8609075 NM_001131019.3:c.259G>T