Allele Registry

Canonical Allele Identifier: PA102910

Gene: GFAP HGNC NCBI

ClinVar RCV:

RCV000056828

RCV000192167

ClinVar Variation:

66434

HGVS (amino-acid)	Matching Registered Transcripts
NP_002046.1:p.Tyr366His	CA217111 NM_002055.5:c.1096T>C