Canonical Allele Identifier: PA2825977277
Gene: FLNB HGNC NCBI

Linked Data

ClinVar Variation Id: 2830849
ClinVar RCV Id: RCV003678880
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157791.1:p.Phe2347Ile
CA353364638
NM_001164319.2:c.7039T>A