Allele Registry

Canonical Allele Identifier: PA102331

Gene: GFAP HGNC NCBI

ClinVar RCV:

RCV000017551

RCV000056899

ClinVar Variation:

16168

HGVS (amino-acid)	Matching Registered Transcripts
NP_002046.1:p.Arg239His	CA217209 NM_002055.5:c.716G>A