Canonical Allele Identifier: PA2825975961
Gene: FLNB HGNC NCBI

Linked Data

ClinVar Variation Id: 346298

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157791.1:p.Glu78Gly
CA2467477
NM_001164319.2:c.233A>G