Canonical Allele Identifier: PA231119
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 129092

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Val1793Met
CA231117
NM_001458.5:c.5377G>A