Allele Registry

Canonical Allele Identifier: PA2826297980

Gene: GFAP HGNC NCBI

ClinVar RCV:

RCV000056870

RCV000192111

ClinVar Variation:

66471

HGVS (amino-acid)	Matching Registered Transcripts
NP_001229305.1:p.Arg79Pro	CA217168 NM_001242376.3:c.236G>C