Canonical Allele Identifier: PA102668
Gene: GFAP HGNC NCBI

Linked Data

ClinVar Variation Id: 66439
ClinVar RCV Id: RCV000056833 RCV000192173
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002046.1:p.Glu373Lys
CA217118
NM_002055.5:c.1117G>A