Canonical Allele Identifier: PA2825615317
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 752113

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Val2661Ile
CA4476424
NM_001127487.2:c.7981G>A