Canonical Allele Identifier: PA2825610441
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 645485

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Arg269Gln
CA369222539
NM_001127487.2:c.806G>A