Allele Registry

Canonical Allele Identifier: PA2825774552

Gene: GFAP HGNC NCBI

ClinVar RCV:

RCV000056821

RCV000192157

ClinVar Variation:

66428

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124491.1:p.Leu357Pro	CA217101 NM_001131019.3:c.1070T>C