Canonical Allele Identifier: PA341846
Gene: FLNB HGNC NCBI

Linked Data

ClinVar Variation Id: 21284
ClinVar RCV Id: RCV000020447

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001448.2:p.Asp1583del
CA341845
NM_001457.4:c.4747_4749del