Canonical Allele Identifier: PA217116
Gene: GFAP HGNC NCBI

Linked Data

ClinVar Variation Id: 66437

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002046.1:p.Glu371Gly
CA217115
NM_002055.5:c.1112A>G