Canonical Allele Identifier: PA2825611134
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1046144
ClinVar RCV Id: RCV001350661
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Ile608Val
CA4474507
NM_001127487.2:c.1822A>G