Canonical Allele Identifier: PA2825615180
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_001120959.1:p.Tyr2530His
CA369219675
NM_001127487.2:c.7588T>C