Canonical Allele Identifier: PA2825611158
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 2924883
ClinVar RCV Id: RCV003788585
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Asp620del
CA2740097553
NM_001127487.2:c.1858_1860del