Canonical Allele Identifier: PA658678492
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 472026

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Arg1008Cys
CA4474936
NM_001458.5:c.3022C>T