Allele Registry

Canonical Allele Identifier: PA2828120176

Gene: GFAP HGNC NCBI

ClinVar RCV:

RCV000017557

RCV000056863

ClinVar Variation:

16174

HGVS (amino-acid)	Matching Registered Transcripts
NP_001350775.1:p.Leu76Phe	CA217160 NM_001363846.2:c.226C>T