Canonical Allele Identifier: PA2828120299
Gene: GFAP HGNC NCBI

Linked Data

ClinVar Variation Id: 1299244
ClinVar RCV Id: RCV001725869

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350775.1:p.Lys236Glu
CA399845737
NM_001363846.2:c.706A>G