Canonical Allele Identifier: PA891850092
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 581430
ClinVar RCV Id: RCV000705249

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Arg2176Cys
CA166191053
NM_001458.5:c.6526C>T