Allele Registry

Canonical Allele Identifier: PA2825973497

Gene: FLNB HGNC NCBI

ClinVar RCV:

RCV000020457

ClinVar Variation:

21294

HGVS (amino-acid)	Matching Registered Transcripts
NP_001157789.1:p.Gln203Pro	CA341862 NM_001164317.2:c.608A>C