Canonical Allele Identifier: PA915988252
Gene: FLNB HGNC NCBI

Linked Data

ClinVar Variation Id: 21286
ClinVar RCV Id: RCV000020449
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157789.1:p.Ser1633Pro
CA341848
NM_001164317.2:c.4897T>C