Allele Registry

Canonical Allele Identifier: PA347192

Gene: GFAP HGNC NCBI

ClinVar RCV:

RCV000192117

RCV001850427

ClinVar Variation:

190339

HGVS (amino-acid)	Matching Registered Transcripts
NP_002046.1:p.Val87Ile	CA347191 NM_002055.5:c.259G>A