Allele Registry

Canonical Allele Identifier: PA2826298203

Gene: GFAP HGNC NCBI

ClinVar RCV:

RCV000056832

RCV000192171

ClinVar Variation:

66438

HGVS (amino-acid)	Matching Registered Transcripts
NP_001229305.1:p.Glu371Val	CA217117 NM_001242376.3:c.1112A>T