Allele Registry

Canonical Allele Identifier: PA2825976028

Gene: FLNB HGNC NCBI

ClinVar RCV:

RCV000020457

ClinVar Variation:

21294

HGVS (amino-acid)	Matching Registered Transcripts
NP_001157791.1:p.Gln203Pro	CA341862 NM_001164319.2:c.608A>C