Canonical Allele Identifier: PA2825975969
Gene: FLNB HGNC NCBI

Linked Data

ClinVar Variation Id: 506644
ClinVar RCV Id: RCV000897835 RCV004543411
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157791.1:p.Ile92Val
CA2467484
NM_001164319.2:c.274A>G