Allele Registry

Canonical Allele Identifier: PA916044552

Gene: GFAP HGNC NCBI

ClinVar RCV:

RCV000056851

RCV000192188

ClinVar Variation:

66456

HGVS (amino-acid)	Matching Registered Transcripts
NP_001350775.1:p.Gln466Leu	CA217144 NM_001363846.2:c.1397A>T