Canonical Allele Identifier: PA658808940
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 539431

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Asn1817del
CA658797013
NM_001458.5:c.5451_5453del