Allele Registry

Canonical Allele Identifier: PA915988262

Gene: FLNB HGNC NCBI

ClinVar RCV:

RCV000020451

ClinVar Variation:

21288

HGVS (amino-acid)	Matching Registered Transcripts
NP_001157789.1:p.Ala1674Ser	CA341851 NM_001164317.2:c.5020G>T