Allele Registry

Canonical Allele Identifier: PA2828120335

Gene: GFAP HGNC NCBI

ClinVar RCV:

RCV000056911

RCV000192149

ClinVar Variation:

66507

HGVS (amino-acid)	Matching Registered Transcripts
NP_001350775.1:p.Lys279Glu	CA217224 NM_001363846.2:c.835A>G