Allele Registry

Canonical Allele Identifier: PA2825774567

Gene: GFAP HGNC NCBI

ClinVar RCV:

RCV000056829

RCV000192168

ClinVar Variation:

66435

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124491.1:p.Tyr366Cys	CA217112 NM_001131019.3:c.1097A>G