Canonical Allele Identifier: PA2825615207
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 949026
ClinVar RCV Id: RCV001220403

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Lys2556Glu
CA369219950
NM_001127487.2:c.7666A>G