Allele Registry

Canonical Allele Identifier: PA2828120216

Gene: GFAP HGNC NCBI

ClinVar RCV:

RCV000056881

RCV000192122

ClinVar Variation:

66480

HGVS (amino-acid)	Matching Registered Transcripts
NP_001350775.1:p.Leu97Pro	CA217185 NM_001363846.2:c.290T>C