Canonical Allele Identifier: PA2829332722
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 3221714
ClinVar RCV Id: RCV004511038

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Val914Phe
CA369193101
NM_001458.5:c.2740G>T