Canonical Allele Identifier: PA2741884797
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 2928153
ClinVar RCV Id: RCV003786975

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Lys2676Glu
CA4476414
NM_001458.5:c.8026A>G