Canonical Allele Identifier: PA2825774589
Gene: GFAP HGNC NCBI

Linked Data

ClinVar Variation Id: 66447
ClinVar RCV Id: RCV000056841 RCV000192178
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124491.1:p.Thr383Ile
CA217128
NM_001131019.3:c.1148C>T