Allele Registry

Canonical Allele Identifier: PA2825774336

Gene: GFAP HGNC NCBI

ClinVar RCV:

RCV000056861

RCV000192102

ClinVar Variation:

66466

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124491.1:p.Met74Thr	CA217158 NM_001131019.3:c.221T>C