Canonical Allele Identifier: PA915988241
Gene: FLNB HGNC NCBI

Linked Data

ClinVar Variation Id: 449027
ClinVar RCV Id: RCV000520108 RCV002476050
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157789.1:p.Ala1608Val
CA2468855
NM_001164317.2:c.4823C>T