Canonical Allele Identifier: PA891849916
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 566030
ClinVar RCV Id: RCV000685741
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Ala934Thr
CA4474841
NM_001458.5:c.2800G>A