Canonical Allele Identifier: PA915984548
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 663566

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Gly2050Glu
CA369211429
NM_001458.5:c.6149G>A