Canonical Allele Identifier: PA658678570
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 472076

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Ala1569Thr
CA4475425
NM_001458.5:c.4705G>A