Canonical Allele Identifier: PA658678609
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 472111

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Arg1931His
CA369208463
NM_001458.5:c.5792G>A