Allele Registry

Canonical Allele Identifier: PA102478

Gene: GFAP HGNC NCBI

ClinVar RCV:

RCV000056871

RCV000192112

ClinVar Variation:

66472

HGVS (amino-acid)	Matching Registered Transcripts
NP_002046.1:p.Arg79Leu	CA217169 NM_002055.5:c.236G>T