Canonical Allele Identifier: PA2825774564
Gene: GFAP HGNC NCBI

Linked Data

ClinVar Variation Id: 66433

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124491.1:p.Ala364Val
CA217109
NM_001131019.3:c.1091C>T