Canonical Allele Identifier: PA2829334511
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 573844
ClinVar RCV Id: RCV000695617

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Pro2725_Ter2726insTrpIleProLysValProProGlnProGlnProProProProAlaThrHisThrLeuHisThrHisThrHisThrHisLysCysAlaThrProArgHisAlaGlnAsnGlnThrLeuGlnThrProAlaLeuGlyValLys
CA369222305
NM_001458.5:c.8178A>G