Allele Registry

Canonical Allele Identifier: PA096492

Gene: FLNB HGNC NCBI

ClinVar RCV:

RCV000030660

RCV002276538

ClinVar Variation:

6398

HGVS (amino-acid)	Matching Registered Transcripts
NP_001448.2:p.Phe161Cys	CA130016 NM_001457.4:c.482T>G