Canonical Allele Identifier: PA2825976280
Gene: FLNB HGNC NCBI

Linked Data

ClinVar Variation Id: 1963840
ClinVar RCV Id: RCV002716206
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157791.1:p.Asn663His
CA353342197
NM_001164319.2:c.1987A>C