Allele Registry

Canonical Allele Identifier: PA915988243

Gene: FLNB HGNC NCBI

ClinVar RCV:

RCV000030661

ClinVar Variation:

6399

HGVS (amino-acid)	Matching Registered Transcripts
NP_001157789.1:p.Gly1617Arg	CA130017 NM_001164317.2:c.4849G>A CA353352098 NM_001164317.2:c.4849G>C