Allele Registry

Canonical Allele Identifier: PA102429

Gene: GFAP HGNC NCBI

ClinVar RCV:

RCV000056856

RCV000192099

ClinVar Variation:

66461

HGVS (amino-acid)	Matching Registered Transcripts
NP_002046.1:p.Arg70Gln	CA217152 NM_002055.5:c.209G>A