Canonical Allele Identifier: PA2826297974
Gene: GFAP HGNC NCBI

Linked Data

ClinVar Variation Id: 66468

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001229305.1:p.Asn77Ser
CA217162
NM_001242376.3:c.230A>G