Allele Registry

Canonical Allele Identifier: PA102764

Gene: GFAP HGNC NCBI

ClinVar RCV:

RCV000056862

RCV000192106

ClinVar Variation:

66467

HGVS (amino-acid)	Matching Registered Transcripts
NP_002046.1:p.Leu76Val	CA217159 NM_002055.5:c.226C>G