Allele Registry

Canonical Allele Identifier: PA2828120191

Gene: GFAP HGNC NCBI

ClinVar RCV:

RCV000056867

RCV000192109

ClinVar Variation:

66470

HGVS (amino-acid)	Matching Registered Transcripts
NP_001350775.1:p.Arg79Gly	CA217165 NM_001363846.2:c.235C>G