Canonical Allele Identifier: PA2573185953
Gene: FLNB HGNC NCBI

Linked Data

ClinVar Variation Id: 1476326
ClinVar RCV Id: RCV001977898

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157789.1:p.Arg1618His
CA2468859
NM_001164317.2:c.4853G>A