Canonical Allele Identifier: PA2825976838
Gene: FLNB HGNC NCBI

Linked Data

ClinVar Variation Id: 1006578
ClinVar RCV Id: RCV001303641

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157791.1:p.Ile1590Thr
CA353352128
NM_001164319.2:c.4769T>C