Canonical Allele Identifier: PA658678511
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 472041

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Gly1197Arg
CA4475074
NM_001458.5:c.3589G>A
CA369197300
NM_001458.5:c.3589G>C