Canonical Allele Identifier: PA2825614282
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 2565527

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Lys2016Asn
CA369211419
NM_001127487.2:c.6048G>C
CA369211421
NM_001127487.2:c.6048G>T