Canonical Allele Identifier: PA2826297910
Gene: GFAP HGNC NCBI

Linked Data

ClinVar Variation Id: 1416421
ClinVar RCV Id: RCV001921246

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001229305.1:p.Arg11His
CA8609128
NM_001242376.3:c.32G>A