Allele Registry

Canonical Allele Identifier: PA2825774568

Gene: GFAP HGNC NCBI

ClinVar RCV:

RCV000056828

RCV000192167

ClinVar Variation:

66434

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124491.1:p.Tyr366His	CA217111 NM_001131019.3:c.1096T>C