Allele Registry

Canonical Allele Identifier: PA915982230

Gene: FLNB HGNC NCBI

ClinVar RCV:

RCV001002590

ClinVar Variation:

812028

HGVS (amino-acid)	Matching Registered Transcripts
NP_001448.2:p.Gly168Cys	CA353333575 NM_001457.4:c.502G>T