Allele Registry

Canonical Allele Identifier: PA2828120372

Gene: GFAP HGNC NCBI

ClinVar RCV:

RCV000056917

ClinVar Variation:

66513

HGVS (amino-acid)	Matching Registered Transcripts
NP_001350775.1:p.Arg330Gly	CA217233 NM_001363846.2:c.988C>G