Canonical Allele Identifier: PA2825614152
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 848238

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Arg1966Trp
CA4475847
NM_001127487.2:c.5896C>T