Allele Registry

Canonical Allele Identifier: PA2826297957

Gene: GFAP HGNC NCBI

ClinVar RCV:

RCV000056856

RCV000192099

ClinVar Variation:

66461

HGVS (amino-acid)	Matching Registered Transcripts
NP_001229305.1:p.Arg70Gln	CA217152 NM_001242376.3:c.209G>A