Allele Registry

Canonical Allele Identifier: PA2825973494

Gene: FLNB HGNC NCBI

ClinVar RCV:

RCV000006771

RCV000006772

ClinVar Variation:

6401

HGVS (amino-acid)	Matching Registered Transcripts
NP_001157789.1:p.Met202Val	CA253857 NM_001164317.2:c.604A>G