Allele Registry

Canonical Allele Identifier: PA2825976018

Gene: FLNB HGNC NCBI

ClinVar RCV:

RCV000413979

RCV001196906

ClinVar Variation:

372794

HGVS (amino-acid)	Matching Registered Transcripts
NP_001157791.1:p.Pro191Leu	CA16042534 NM_001164319.2:c.572C>T