Allele Registry

Canonical Allele Identifier: PA2826297989

Gene: GFAP HGNC NCBI

ClinVar RCV:

RCV002508567

ClinVar Variation:

1810011

HGVS (amino-acid)	Matching Registered Transcripts
NP_001229305.1:p.Tyr83Asn	CA291034264 NM_001242376.3:c.247T>A