Canonical Allele Identifier: PA2825975338
Gene: FLNB HGNC NCBI

Linked Data

ClinVar Variation Id: 1423798
ClinVar RCV Id: RCV001929097 RCV002276936
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157790.1:p.Thr1579Ile
CA353352056
NM_001164318.2:c.4736C>T