Canonical Allele Identifier: PA1139704474
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 861277

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Gly2054Arg
CA369211469
NM_001458.5:c.6160G>A
CA369211472
NM_001458.5:c.6160G>C