Canonical Allele Identifier: PA2741839094
Gene: FLNB HGNC NCBI

Linked Data

ClinVar Variation Id: 2976386
ClinVar RCV Id: RCV003836536
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157789.1:p.Thr1651Met
CA2468877
NM_001164317.2:c.4952C>T