Canonical Allele Identifier: PA102573
Gene: GFAP HGNC NCBI

Linked Data

ClinVar Variation Id: 66492
ClinVar RCV Id: RCV000056893 RCV000192129
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002046.1:p.Glu207Gln
CA217202
NM_002055.5:c.619G>C