Canonical Allele Identifier: PA658654682
Gene: FLNB HGNC NCBI

Linked Data

ClinVar Variation Id: 440969
ClinVar RCV Id: RCV000509290
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001448.2:p.Thr1620Lys
CA353352308
NM_001457.4:c.4859C>A