Allele Registry

Canonical Allele Identifier: PA2828120181

Gene: GFAP HGNC NCBI

ClinVar RCV:

RCV000056865

RCV000192107

ClinVar Variation:

66468

HGVS (amino-acid)	Matching Registered Transcripts
NP_001350775.1:p.Asn77Ser	CA217162 NM_001363846.2:c.230A>G