Canonical Allele Identifier: PA2825977029
Gene: FLNB HGNC NCBI

Linked Data

ClinVar Variation Id: 346353

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157791.1:p.Glu1949Lys
CA2469211
NM_001164319.2:c.5845G>A