Allele Registry

Canonical Allele Identifier: PA2826298181

Gene: GFAP HGNC NCBI

ClinVar RCV:

RCV000056821

RCV000192157

ClinVar Variation:

66428

HGVS (amino-acid)	Matching Registered Transcripts
NP_001229305.1:p.Leu357Pro	CA217101 NM_001242376.3:c.1070T>C