Canonical Allele Identifier: PA2741884800
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 2935438
ClinVar RCV Id: RCV003791092

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Val2684Met
CA369221421
NM_001458.5:c.8050G>A