Allele Registry

Canonical Allele Identifier: PA2825774329

Gene: GFAP HGNC NCBI

ClinVar RCV:

RCV000414950

ClinVar Variation:

374303

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124491.1:p.Glu72Gly	CA16043694 NM_001131019.3:c.215A>G