Allele Registry

Canonical Allele Identifier: PA2825973689

Gene: FLNB HGNC NCBI

ClinVar RCV:

RCV000443161

RCV002522689

ClinVar Variation:

392383

HGVS (amino-acid)	Matching Registered Transcripts
NP_001157789.1:p.His560Arg	CA2467895 NM_001164317.2:c.1679A>G