Allele Registry

Canonical Allele Identifier: PA2826298009

Gene: GFAP HGNC NCBI

ClinVar RCV:

RCV000056881

RCV000192122

ClinVar Variation:

66480

HGVS (amino-acid)	Matching Registered Transcripts
NP_001229305.1:p.Leu97Pro	CA217185 NM_001242376.3:c.290T>C