Canonical Allele Identifier: PA915988250
Gene: FLNB HGNC NCBI

Linked Data

ClinVar Variation Id: 346345

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157789.1:p.Met1620Lys
CA2468860
NM_001164317.2:c.4859T>A