Allele Registry

Canonical Allele Identifier: PA2825774341

Gene: GFAP HGNC NCBI

ClinVar RCV:

RCV000017558

RCV000056864

ClinVar Variation:

16175

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124491.1:p.Asn77Tyr	CA217161 NM_001131019.3:c.229A>T