Allele Registry

Canonical Allele Identifier: PA102449

Gene: GFAP HGNC NCBI

ClinVar RCV:

RCV000017554

RCV000056868

ClinVar Variation:

16171

HGVS (amino-acid)	Matching Registered Transcripts
NP_002046.1:p.Arg79Cys	CA217166 NM_002055.5:c.235C>T