Canonical Allele Identifier: PA102376
Gene: GFAP HGNC NCBI

Linked Data

ClinVar Variation Id: 16177

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002046.1:p.Arg276Leu
CA217223
NM_002055.5:c.827G>T