Allele Registry

Canonical Allele Identifier: PA102697

Gene: GFAP HGNC NCBI

ClinVar RCV:

RCV000056858

RCV000192101

ClinVar Variation:

66463

HGVS (amino-acid)	Matching Registered Transcripts
NP_002046.1:p.Glu72Lys	CA217155 NM_002055.5:c.214G>A