Canonical Allele Identifier: PA2828120409
Gene: GFAP HGNC NCBI

Linked Data

ClinVar Variation Id: 66438

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350775.1:p.Glu371Val
CA217117
NM_001363846.2:c.1112A>T