Canonical Allele Identifier: PA1139703053
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 938780

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Arg1150Trp
CA4475041
NM_001458.5:c.3448C>T