Canonical Allele Identifier: PA891849837
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 580201
ClinVar RCV Id: RCV000703671 RCV002406641 RCV002477623
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Ser589Leu
CA4474469
NM_001458.5:c.1766C>T