Canonical Allele Identifier: PA2580262550
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 2264304
ClinVar RCV Id: RCV004122336
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Ile821Val
CA369191668
NM_001458.5:c.2461A>G