Canonical Allele Identifier: PA2828120386
Gene: GFAP HGNC NCBI

Linked Data

ClinVar Variation Id: 16178

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350775.1:p.Leu352Pro
CA217100
NM_001363846.2:c.1055T>C