Canonical Allele Identifier: PA1139704643
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 854256

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Thr2177Asn
CA4476007
NM_001458.5:c.6530C>A