Canonical Allele Identifier: PA2825615238
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1017007

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Val2581Met
CA4476373
NM_001127487.2:c.7741G>A