Canonical Allele Identifier: PA2825611102
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 580201

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Ser589Leu
CA4474469
NM_001127487.2:c.1766C>T