Canonical Allele Identifier: PA2826298219
Gene: GFAP HGNC NCBI

Linked Data

ClinVar Variation Id: 66447
ClinVar RCV Id: RCV000056841 RCV000192178
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001229305.1:p.Thr383Ile
CA217128
NM_001242376.3:c.1148C>T