Allele Registry

Canonical Allele Identifier: PA102573

Gene: GFAP HGNC NCBI

ClinVar RCV:

RCV000056893

RCV000192129

ClinVar Variation:

66492

HGVS (amino-acid)	Matching Registered Transcripts
NP_002046.1:p.Glu207Gln	CA217202 NM_002055.5:c.619G>C