Allele Registry

Canonical Allele Identifier: PA2826298001

Gene: GFAP HGNC NCBI

ClinVar RCV:

RCV000017555

RCV000056879

ClinVar Variation:

16172

HGVS (amino-acid)	Matching Registered Transcripts
NP_001229305.1:p.Arg88Cys	CA217183 NM_001242376.3:c.262C>T