Canonical Allele Identifier: PA2828120346
Gene: GFAP HGNC NCBI

Linked Data

ClinVar Variation Id: 190350
ClinVar RCV Id: RCV000192150

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350775.1:p.Gln290Glu
CA347212
NM_001363846.2:c.868C>G