Canonical Allele Identifier: PA2825611166
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1717319
ClinVar RCV Id: RCV002304757

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Lys621Met
CA369227238
NM_001127487.2:c.1862A>T