Allele Registry

Canonical Allele Identifier: PA2828120211

Gene: GFAP HGNC NCBI

ClinVar RCV:

RCV000056880

RCV000192120

ClinVar Variation:

66479

HGVS (amino-acid)	Matching Registered Transcripts
NP_001350775.1:p.Leu90Pro	CA217184 NM_001363846.2:c.269T>C