Canonical Allele Identifier: PA2573217848
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1510639

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Thr2188Met
CA4476016
NM_001458.5:c.6563C>T