Allele Registry

Canonical Allele Identifier: PA2825774484

Gene: GFAP HGNC NCBI

ClinVar RCV:

RCV000056907

RCV000192142

ClinVar Variation:

66504

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124491.1:p.Tyr257Cys	CA217220 NM_001131019.3:c.770A>G