Canonical Allele Identifier: PA2741884559
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 2929498
ClinVar RCV Id: RCV003784664

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Ile608Phe
CA166217101
NM_001458.5:c.1822A>T