Canonical Allele Identifier: PA2825774459
Gene: GFAP HGNC NCBI

Linked Data

ClinVar Variation Id: 1032795
ClinVar RCV Id: RCV001334994
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124491.1:p.Ala233Thr
CA399845768
NM_001131019.3:c.697G>A