Allele Registry

Canonical Allele Identifier: PA2825774469

Gene: GFAP HGNC NCBI

ClinVar RCV:

RCV000017550

RCV000056898

ClinVar Variation:

16167

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124491.1:p.Arg239Cys	CA217208 NM_001131019.3:c.715C>T