Allele Registry

Canonical Allele Identifier: PA102601

Gene: GFAP HGNC NCBI

ClinVar RCV:

RCV000056919

RCV000192154

ClinVar Variation:

66515

HGVS (amino-acid)	Matching Registered Transcripts
NP_002046.1:p.Glu332Lys	CA217236 NM_002055.5:c.994G>A