Canonical Allele Identifier: PA102634
Gene: GFAP HGNC NCBI

Linked Data

ClinVar Variation Id: 66438
ClinVar RCV Id: RCV000056832 RCV000192171
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002046.1:p.Glu371Val
CA217117
NM_002055.5:c.1112A>T