Canonical Allele Identifier: PA2825976831
Gene: FLNB HGNC NCBI

Linked Data

ClinVar Variation Id: 21284
ClinVar RCV Id: RCV000020447
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157791.1:p.Asp1583del
CA341845
NM_001164319.2:c.4747_4749del