Canonical Allele Identifier: PA915985039
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 752113

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Val2694Ile
CA4476424
NM_001458.5:c.8080G>A