Canonical Allele Identifier: PA2829330932
Gene: FLNB HGNC NCBI

Linked Data

ClinVar Variation Id: 2830849
ClinVar RCV Id: RCV003678880
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001448.2:p.Phe2371Ile
CA353364638
NM_001457.4:c.7111T>A