Allele Registry

Canonical Allele Identifier: PA102793

Gene: GFAP HGNC NCBI

ClinVar RCV:

RCV000056897

RCV000192134

ClinVar Variation:

66496

HGVS (amino-acid)	Matching Registered Transcripts
NP_002046.1:p.Lys236Thr	CA217207 NM_002055.5:c.707A>C