Canonical Allele Identifier: PA2826297981
Gene: GFAP HGNC NCBI

Linked Data

ClinVar Variation Id: 66472

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001229305.1:p.Arg79Leu
CA217169
NM_001242376.3:c.236G>T