Canonical Allele Identifier: PA2573185949
Gene: FLNB HGNC NCBI

Linked Data

ClinVar Variation Id: 1423798

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157789.1:p.Thr1610Ile
CA353352056
NM_001164317.2:c.4829C>T