Allele Registry

Canonical Allele Identifier: PA2825973502

Gene: FLNB HGNC NCBI

ClinVar RCV:

RCV000020458

ClinVar Variation:

21295

HGVS (amino-acid)	Matching Registered Transcripts
NP_001157789.1:p.Gly210Val	CA341864 NM_001164317.2:c.629G>T