Canonical Allele Identifier: PA2825974063
Gene: FLNB HGNC NCBI

Linked Data

ClinVar Variation Id: 346334
ClinVar RCV Id: RCV000349068 RCV000915285 RCV002502330 RCV002278561
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157789.1:p.Val1195Met
CA2468451
NM_001164317.2:c.3583G>A