Canonical Allele Identifier: PA2825774571
Gene: GFAP HGNC NCBI

Linked Data

ClinVar Variation Id: 1077122
ClinVar RCV Id: RCV001391254

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124491.1:p.Leu370Pro
CA399843384
NM_001131019.3:c.1109T>C