Canonical Allele Identifier: PA2825774282
Gene: GFAP HGNC NCBI

Linked Data

ClinVar Variation Id: 1420224
ClinVar RCV Id: RCV001914113
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124491.1:p.Arg11Pro
CA399849223
NM_001131019.3:c.32G>C