Canonical Allele Identifier: PA2580262492
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1773787
ClinVar RCV Id: RCV002389704

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Phe497Leu
CA369225698
NM_001458.5:c.1489T>C
CA369225708
NM_001458.5:c.1491C>A
CA369225710
NM_001458.5:c.1491C>G