Allele Registry

Canonical Allele Identifier: PA341858

Gene: FLNB HGNC NCBI

ClinVar RCV:

RCV000020454

ClinVar Variation:

21291

HGVS (amino-acid)	Matching Registered Transcripts
NP_001448.2:p.Cys183Trp	CA341857 NM_001457.4:c.549C>G