Canonical Allele Identifier: PA2825614470
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 840155

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Gly2118Ser
CA369212569
NM_001127487.2:c.6352G>A