Allele Registry

Canonical Allele Identifier: PA2825974720

Gene: FLNB HGNC NCBI

ClinVar Allele:

359592

ClinVar RCV:

RCV000412741

RCV002480263

RCV002523908

ClinVar Variation:

372367

HGVS (amino-acid)	Matching Registered Transcripts
NP_001157790.1:p.Gly530Trp	CA2467856 NM_001164318.2:c.1588G>T