Canonical Allele Identifier: PA2825612036
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 472026

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Arg1008Cys
CA4474936
NM_001127487.2:c.3022C>T