Canonical Allele Identifier: PA2825611116
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1419843
ClinVar RCV Id: RCV001910664

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Val601Met
CA4474479
NM_001127487.2:c.1801G>A