Canonical Allele Identifier: PA2825615200
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 472180

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Gly2545Ser
CA4476342
NM_001127487.2:c.7633G>A