Allele Registry

Canonical Allele Identifier: PA2826298098

Gene: GFAP HGNC NCBI

ClinVar RCV:

RCV000056900

RCV000192136

ClinVar Variation:

66497

HGVS (amino-acid)	Matching Registered Transcripts
NP_001229305.1:p.Arg239Pro	CA217210 NM_001242376.3:c.716G>C