Canonical Allele Identifier: PA2829331119
Gene: FLNB HGNC NCBI

Linked Data

ClinVar Variation Id: 2441475
ClinVar RCV Id: RCV003144016
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001448.2:p.Phe2526Tyr
CA2469726
NM_001457.4:c.7577T>A