Canonical Allele Identifier: PA2825612397
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1936408
ClinVar RCV Id: RCV002636401
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Phe1153Tyr
CA369196968
NM_001127487.2:c.3458T>A