Canonical Allele Identifier: PA2580262858
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1758119
ClinVar RCV Id: RCV002382694

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Gln2432Lys
CA369216624
NM_001458.5:c.7294C>A