Canonical Allele Identifier: PA2825976286
Gene: FLNB HGNC NCBI

Linked Data

ClinVar Variation Id: 618659
ClinVar RCV Id: RCV000757317 RCV004527772
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157791.1:p.Thr669Ala
CA2467995
NM_001164319.2:c.2005A>G