Canonical Allele Identifier: PA2825973458
Gene: FLNB HGNC NCBI

Linked Data

ClinVar Variation Id: 1718781
ClinVar RCV Id: RCV002301689
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157789.1:p.Ile158Val
CA353333501
NM_001164317.2:c.472A>G