Canonical Allele Identifier: PA2825973753
Gene: FLNB HGNC NCBI

Linked Data

ClinVar Variation Id: 618659

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157789.1:p.Thr669Ala
CA2467995
NM_001164317.2:c.2005A>G