Allele Registry

Canonical Allele Identifier: PA2825774338

Gene: GFAP HGNC NCBI

ClinVar RCV:

RCV000056862

RCV000192106

ClinVar Variation:

66467

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124491.1:p.Leu76Val	CA217159 NM_001131019.3:c.226C>G