Allele Registry

Canonical Allele Identifier: PA2828120189

Gene: GFAP HGNC NCBI

ClinVar RCV:

RCV000056871

RCV000192112

ClinVar Variation:

66472

HGVS (amino-acid)	Matching Registered Transcripts
NP_001350775.1:p.Arg79Leu	CA217169 NM_001363846.2:c.236G>T