Allele Registry

Canonical Allele Identifier: PA217192

Gene: GFAP HGNC NCBI

ClinVar RCV:

RCV000056885

RCV000192126

ClinVar Variation:

66484

HGVS (amino-acid)	Matching Registered Transcripts
NP_002046.1:p.Asp128Asn	CA217191 NM_002055.5:c.382G>A