Allele Registry

Canonical Allele Identifier: PA2825774465

Gene: GFAP HGNC NCBI

ClinVar RCV:

RCV000056901

RCV000192137

ClinVar Variation:

66498

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124491.1:p.Arg239Leu	CA217211 NM_001131019.3:c.716G>T