Canonical Allele Identifier: PA891850123
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 572053

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Arg2553Gln
CA4476334
NM_001458.5:c.7658G>A