Canonical Allele Identifier: PA2825615177
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 648299
ClinVar RCV Id: RCV000803002

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Val2527Ala
CA166195470
NM_001127487.2:c.7580T>C