Canonical Allele Identifier: PA658808589
Gene: FLNB HGNC NCBI

Linked Data

ClinVar Variation Id: 523615
ClinVar RCV Id: RCV000627040
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001448.2:p.Ser778Gly
CA353343971
NM_001457.4:c.2332A>G