Allele Registry

Canonical Allele Identifier: PA2828120279

Gene: GFAP HGNC NCBI

ClinVar RCV:

RCV000056892

RCV000192128

ClinVar Variation:

66491

HGVS (amino-acid)	Matching Registered Transcripts
NP_001350775.1:p.Glu207Lys	CA217201 NM_001363846.2:c.619G>A