Canonical Allele Identifier: PA2828120138
Gene: GFAP HGNC NCBI

Linked Data

ClinVar Variation Id: 2498708
ClinVar RCV Id: RCV003222917

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350775.1:p.Arg30Cys
CA8609110
NM_001363846.2:c.88C>T