Allele Registry

Canonical Allele Identifier: PA2828120180

Gene: GFAP HGNC NCBI

ClinVar RCV:

RCV000017558

RCV000056864

ClinVar Variation:

16175

HGVS (amino-acid)	Matching Registered Transcripts
NP_001350775.1:p.Asn77Tyr	CA217161 NM_001363846.2:c.229A>T