Allele Registry

Canonical Allele Identifier: PA2828120321

Gene: GFAP HGNC NCBI

ClinVar RCV:

RCV000056907

RCV000192142

ClinVar Variation:

66504

HGVS (amino-acid)	Matching Registered Transcripts
NP_001350775.1:p.Tyr257Cys	CA217220 NM_001363846.2:c.770A>G