Allele Registry

Canonical Allele Identifier: PA916044550

Gene: GFAP HGNC NCBI

ClinVar RCV:

RCV000056849

RCV000192186

ClinVar Variation:

66454

HGVS (amino-acid)	Matching Registered Transcripts
NP_001350775.1:p.Asp457Ala	CA217141 NM_001363846.2:c.1370A>C