Canonical Allele Identifier: PA2826297914
Gene: GFAP HGNC NCBI

Linked Data

ClinVar Variation Id: 1974786
ClinVar RCV Id: RCV002765796

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001229305.1:p.Arg12Gly
CA399849220
NM_001242376.3:c.34C>G