Canonical Allele Identifier: PA2825611841
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 570761

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Arg916Gln
CA4474835
NM_001127487.2:c.2747G>A