Allele Registry

Canonical Allele Identifier: PA102333

Gene: GFAP HGNC NCBI

ClinVar RCV:

RCV000056901

RCV000192137

ClinVar Variation:

66498

HGVS (amino-acid)	Matching Registered Transcripts
NP_002046.1:p.Arg239Leu	CA217211 NM_002055.5:c.716G>T