Canonical Allele Identifier: PA658808960
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 539403
ClinVar RCV Id: RCV000649133

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Cys2154Ser
CA369212589
NM_001458.5:c.6460T>A
CA369212593
NM_001458.5:c.6461G>C