Allele Registry

Canonical Allele Identifier: PA2825976013

Gene: FLNB HGNC NCBI

ClinVar RCV:

RCV000020454

ClinVar Variation:

21291

HGVS (amino-acid)	Matching Registered Transcripts
NP_001157791.1:p.Cys183Trp	CA341857 NM_001164319.2:c.549C>G