Canonical Allele Identifier: PA2825774461
Gene: GFAP HGNC NCBI

Linked Data

ClinVar Variation Id: 66495

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124491.1:p.Leu235Pro
CA217206
NM_001131019.3:c.704T>C