Canonical Allele Identifier: PA2825975348
Gene: FLNB HGNC NCBI

Linked Data

ClinVar Variation Id: 1006578
ClinVar RCV Id: RCV001303641
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157790.1:p.Ile1590Thr
CA353352128
NM_001164318.2:c.4769T>C