Canonical Allele Identifier: PA2825976068
Gene: FLNB HGNC NCBI

Linked Data

ClinVar Variation Id: 252548

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157791.1:p.Met270Val
CA2467638
NM_001164319.2:c.808A>G