Canonical Allele Identifier: PA2573217913
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1465459
ClinVar RCV Id: RCV001963715

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Val2708Ile
CA369221920
NM_001458.5:c.8122G>A
CA2573141646
NM_001458.5:c.8121_8122delinsCA