Canonical Allele Identifier: PA2825973476
Gene: FLNB HGNC NCBI

Linked Data

ClinVar Variation Id: 6400

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157789.1:p.Ala173Val
CA253856
NM_001164317.2:c.518C>T