Canonical Allele Identifier: PA2828120141
Gene: GFAP HGNC NCBI

Linked Data

ClinVar Variation Id: 2053943
ClinVar RCV Id: RCV002922899

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350775.1:p.Arg36His
CA8609102
NM_001363846.2:c.107G>A