Canonical Allele Identifier: PA102316
Gene: GFAP HGNC NCBI

Linked Data

ClinVar Variation Id: 16167

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002046.1:p.Arg239Cys
CA217208
NM_002055.5:c.715C>T