Canonical Allele Identifier: PA2825976835
Gene: FLNB HGNC NCBI

Linked Data

ClinVar Variation Id: 1476326
ClinVar RCV Id: RCV001977898
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157791.1:p.Arg1587His
CA2468859
NM_001164319.2:c.4760G>A