Allele Registry

Canonical Allele Identifier: PA645471392

Gene: FLNB HGNC NCBI

ClinVar RCV:

RCV000362857

RCV001753815

RCV004021926

ClinVar Variation:

346367

HGVS (amino-acid)	Matching Registered Transcripts
NP_001448.2:p.Ala2512Thr	CA2469716 NM_001457.4:c.7534G>A