Canonical Allele Identifier: PA2825774441
Gene: GFAP HGNC NCBI

Linked Data

ClinVar Variation Id: 66492

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124491.1:p.Glu207Gln
CA217202
NM_001131019.3:c.619G>C