Canonical Allele Identifier: PA2580262512
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1717319
ClinVar RCV Id: RCV002304757

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Lys621Met
CA369227238
NM_001458.5:c.1862A>T