Canonical Allele Identifier: PA2828120402
Gene: GFAP HGNC NCBI

Linked Data

ClinVar Variation Id: 66433

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350775.1:p.Ala364Val
CA217109
NM_001363846.2:c.1091C>T