Allele Registry

Canonical Allele Identifier: PA217102

Gene: GFAP HGNC NCBI

ClinVar RCV:

RCV000056821

RCV000192157

ClinVar Variation:

66428

HGVS (amino-acid)	Matching Registered Transcripts
NP_002046.1:p.Leu357Pro	CA217101 NM_002055.5:c.1070T>C