Canonical Allele Identifier: PA2825974786
Gene: FLNB HGNC NCBI

Linked Data

ClinVar Variation Id: 288568
ClinVar RCV Id: RCV000353068 RCV001148579 RCV002519308
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157790.1:p.Arg649Gln
CA2467983
NM_001164318.2:c.1946G>A