Canonical Allele Identifier: PA2825774279
Gene: GFAP HGNC NCBI

Linked Data

ClinVar Variation Id: 2130747
ClinVar RCV Id: RCV003047848
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124491.1:p.Thr7del
CA8609132
NM_001131019.3:c.19_21del