Allele Registry

Canonical Allele Identifier: PA2826298080

Gene: GFAP HGNC NCBI

ClinVar RCV:

RCV000056895

RCV000192131

ClinVar Variation:

66494

HGVS (amino-acid)	Matching Registered Transcripts
NP_001229305.1:p.Glu223Gln	CA217204 NM_001242376.3:c.667G>C CA356591 NM_001242376.3:c.[667G>C;236G>A]