Allele Registry

Canonical Allele Identifier: PA102499

Gene: GFAP HGNC NCBI

ClinVar RCV:

RCV000017555

RCV000056879

ClinVar Variation:

16172

HGVS (amino-acid)	Matching Registered Transcripts
NP_002046.1:p.Arg88Cys	CA217183 NM_002055.5:c.262C>T