Canonical Allele Identifier: PA2580262880
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1760424

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Ile2583Thr
CA369219911
NM_001458.5:c.7748T>C