Canonical Allele Identifier: PA2829330166
Gene: FLNB HGNC NCBI

Linked Data

ClinVar Variation Id: 1427376
ClinVar RCV Id: RCV001964600
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001448.2:p.Thr1611Met
CA2468874
NM_001457.4:c.4832C>T