Canonical Allele Identifier: PA2825612959
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1506433

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Lys1394Glu
CA369200530
NM_001127487.2:c.4180A>G