Canonical Allele Identifier: PA2825976847
Gene: FLNB HGNC NCBI

Linked Data

ClinVar Variation Id: 1333671

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157791.1:p.Ser1602Tyr
CA353352200
NM_001164319.2:c.4805C>A