Canonical Allele Identifier: PA915985040
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 641761

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Thr2697Ala
CA369221696
NM_001458.5:c.8089A>G