Canonical Allele Identifier: PA2825613167
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 2161895

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Val1503Ile
CA369201905
NM_001127487.2:c.4507G>A