Allele Registry

Canonical Allele Identifier: PA645470613

Gene: FLNB HGNC NCBI

ClinVar Allele:

359592

ClinVar RCV:

RCV000412741

RCV002480263

RCV002523908

ClinVar Variation:

372367

HGVS (amino-acid)	Matching Registered Transcripts
NP_001448.2:p.Gly530Trp	CA2467856 NM_001457.4:c.1588G>T