Allele Registry

Canonical Allele Identifier: PA102655

Gene: GFAP HGNC NCBI

ClinVar RCV:

RCV000056834

RCV000192174

ClinVar Variation:

66440

HGVS (amino-acid)	Matching Registered Transcripts
NP_002046.1:p.Glu373Gln	CA217119 NM_002055.5:c.1117G>C