Allele Registry

Canonical Allele Identifier: PA2828120305

Gene: GFAP HGNC NCBI

ClinVar RCV:

RCV000056901

RCV000192137

ClinVar Variation:

66498

HGVS (amino-acid)	Matching Registered Transcripts
NP_001350775.1:p.Arg239Leu	CA217211 NM_001363846.2:c.716G>T