Canonical Allele Identifier: PA915984962
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 636988
ClinVar RCV Id: RCV000788970
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Tyr2563His
CA369219675
NM_001458.5:c.7687T>C