Allele Registry

Canonical Allele Identifier: PA2828120194

Gene: GFAP HGNC NCBI

ClinVar RCV:

RCV002508567

ClinVar Variation:

1810011

HGVS (amino-acid)	Matching Registered Transcripts
NP_001350775.1:p.Tyr83Asn	CA291034264 NM_001363846.2:c.247T>A