Allele Registry

Canonical Allele Identifier: PA2825976001

Gene: FLNB HGNC NCBI

ClinVar RCV:

RCV001002590

ClinVar Variation:

812028

HGVS (amino-acid)	Matching Registered Transcripts
NP_001157791.1:p.Gly168Cys	CA353333575 NM_001164319.2:c.502G>T