Allele Registry

Canonical Allele Identifier: PA2828120179

Gene: GFAP HGNC NCBI

ClinVar RCV:

RCV002043282

ClinVar Variation:

1511262

HGVS (amino-acid)	Matching Registered Transcripts
NP_001350775.1:p.Asn77Asp	CA399848709 NM_001363846.2:c.229A>G