Canonical Allele Identifier: PA2580262789
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1925266
ClinVar RCV Id: RCV002618125

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Val2084Leu
CA369211903
NM_001458.5:c.6250G>T
CA369211904
NM_001458.5:c.6250G>C