Allele Registry

Canonical Allele Identifier: PA102624

Gene: GFAP HGNC NCBI

ClinVar RCV:

RCV000056830

RCV000192169

ClinVar Variation:

66436

HGVS (amino-acid)	Matching Registered Transcripts
NP_002046.1:p.Glu371Gln	CA217114 NM_002055.5:c.1111G>C