Canonical Allele Identifier: PA2828120187
Gene: GFAP HGNC NCBI

Linked Data

ClinVar Variation Id: 66469
ClinVar RCV Id: RCV000056866

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350775.1:p.Arg79Ser
CA217163
NM_001363846.2:c.235C>A