Allele Registry

Canonical Allele Identifier: PA2826298097

Gene: GFAP HGNC NCBI

ClinVar RCV:

RCV000056901

RCV000192137

ClinVar Variation:

66498

HGVS (amino-acid)	Matching Registered Transcripts
NP_001229305.1:p.Arg239Leu	CA217211 NM_001242376.3:c.716G>T