Canonical Allele Identifier: PA2825611143
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1004530

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Ala614Thr
CA4474514
NM_001127487.2:c.1840G>A