Allele Registry

Canonical Allele Identifier: PA2825774574

Gene: GFAP HGNC NCBI

ClinVar RCV:

RCV000056830

RCV000192169

ClinVar Variation:

66436

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124491.1:p.Glu371Gln	CA217114 NM_001131019.3:c.1111G>C