Canonical Allele Identifier: PA2580262805
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 2112094

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Ile2160Thr
CA369212634
NM_001458.5:c.6479T>C