Canonical Allele Identifier: PA2825774288
Gene: GFAP HGNC NCBI

Linked Data

ClinVar Variation Id: 2153444
ClinVar RCV Id: RCV003077619

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124491.1:p.Val15Leu
CA8609124
NM_001131019.3:c.43G>C