Canonical Allele Identifier: PA2825974578
Gene: FLNB HGNC NCBI

Linked Data

ClinVar Variation Id: 252548
ClinVar RCV Id: RCV000238833 RCV000726545 RCV000765752 RCV001148468 RCV002277596 RCV002518511
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157790.1:p.Met270Val
CA2467638
NM_001164318.2:c.808A>G