Canonical Allele Identifier: PA2825612579
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 966556

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Arg1241His
CA4475107
NM_001127487.2:c.3722G>A