Canonical Allele Identifier: PA2826298138
Gene: GFAP HGNC NCBI

Linked Data

ClinVar Variation Id: 190350
ClinVar RCV Id: RCV000192150

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001229305.1:p.Gln290Glu
CA347212
NM_001242376.3:c.868C>G