Canonical Allele Identifier: PA658809026
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 539438

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Asp2551His
CA369219517
NM_001458.5:c.7651G>C