Allele Registry

Canonical Allele Identifier: PA2826298186

Gene: GFAP HGNC NCBI

ClinVar RCV:

RCV000056823

RCV000192161

ClinVar Variation:

66430

HGVS (amino-acid)	Matching Registered Transcripts
NP_001229305.1:p.Leu359Pro	CA217104 NM_001242376.3:c.1076T>C