Allele Registry

Canonical Allele Identifier: PA2828120190

Gene: GFAP HGNC NCBI

ClinVar RCV:

RCV000017553

RCV000056869

ClinVar Variation:

16170

HGVS (amino-acid)	Matching Registered Transcripts
NP_001350775.1:p.Arg79His	CA217167 NM_001363846.2:c.236G>A