Canonical Allele Identifier: PA2499258036
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1011887

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Phe1238Ser
CA4475105
NM_001458.5:c.3713T>C