Allele Registry

Canonical Allele Identifier: PA2825973799

Gene: FLNB HGNC NCBI

ClinVar RCV:

RCV000006773

RCV000508566

ClinVar Variation:

6402

HGVS (amino-acid)	Matching Registered Transcripts
NP_001157789.1:p.Gly751Arg	CA253858 NM_001164317.2:c.2251G>C