Canonical Allele Identifier: PA2826298089
Gene: GFAP HGNC NCBI

Linked Data

ClinVar Variation Id: 1032795
ClinVar RCV Id: RCV001334994

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001229305.1:p.Ala233Thr
CA399845768
NM_001242376.3:c.697G>A