Canonical Allele Identifier: PA2829330907
Gene: FLNB HGNC NCBI

Linked Data

ClinVar Variation Id: 1417463
ClinVar RCV Id: RCV001948151 RCV002556442
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001448.2:p.Arg2346Cys
CA2469592
NM_001457.4:c.7036C>T