Canonical Allele Identifier: PA2499258192
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1017007

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Val2614Met
CA4476373
NM_001458.5:c.7840G>A