Canonical Allele Identifier: PA2573217686
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1415142

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Arg916Trp
CA4474834
NM_001458.5:c.2746C>T