Allele Registry

Canonical Allele Identifier: PA102468

Gene: GFAP HGNC NCBI

ClinVar RCV:

RCV000017553

RCV000056869

ClinVar Variation:

16170

HGVS (amino-acid)	Matching Registered Transcripts
NP_002046.1:p.Arg79His	CA217167 NM_002055.5:c.236G>A