Canonical Allele Identifier: PA2826297962
Gene: GFAP HGNC NCBI

Linked Data

ClinVar Variation Id: 190334
ClinVar RCV Id: RCV000192103

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001229305.1:p.Met73Thr
CA347186
NM_001242376.3:c.218T>C