Allele Registry

Canonical Allele Identifier: PA2826298099

Gene: GFAP HGNC NCBI

ClinVar RCV:

RCV000017551

RCV000056899

ClinVar Variation:

16168

HGVS (amino-acid)	Matching Registered Transcripts
NP_001229305.1:p.Arg239His	CA217209 NM_001242376.3:c.716G>A