Canonical Allele Identifier: PA2825614572
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1510639

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Thr2155Met
CA4476016
NM_001127487.2:c.6464C>T