Canonical Allele Identifier: PA2573080688
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1314338

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.His2023Arg
CA369211143
NM_001458.5:c.6068A>G