Canonical Allele Identifier: PA2825977262
Gene: FLNB HGNC NCBI

Linked Data

ClinVar Variation Id: 1417463
ClinVar RCV Id: RCV001948151 RCV002556442
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157791.1:p.Arg2322Cys
CA2469592
NM_001164319.2:c.6964C>T