Canonical Allele Identifier: PA2825774342
Gene: GFAP HGNC NCBI

Linked Data

ClinVar Variation Id: 66468

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124491.1:p.Asn77Ser
CA217162
NM_001131019.3:c.230A>G