Canonical Allele Identifier: PA2825976102
Gene: FLNB HGNC NCBI

Linked Data

ClinVar Variation Id: 432006

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157791.1:p.Gly361Asp
CA353335772
NM_001164319.2:c.1082G>A