Canonical Allele Identifier: PA2825976861
Gene: FLNB HGNC NCBI

Linked Data

ClinVar Variation Id: 2976386
ClinVar RCV Id: RCV003836536

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157791.1:p.Thr1620Met
CA2468877
NM_001164319.2:c.4859C>T