Canonical Allele Identifier: PA2825774331
Gene: GFAP HGNC NCBI

Linked Data

ClinVar Variation Id: 2132009
ClinVar RCV Id: RCV003062100

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124491.1:p.Met73Ile
CA399848751
NM_001131019.3:c.219G>T
CA399848753
NM_001131019.3:c.219G>C
CA399848755
NM_001131019.3:c.219G>A