Canonical Allele Identifier: PA2826297979
Gene: GFAP HGNC NCBI

Linked Data

ClinVar Variation Id: 66469
ClinVar RCV Id: RCV000056866

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001229305.1:p.Arg79Ser
CA217163
NM_001242376.3:c.235C>A