Canonical Allele Identifier: PA2580262806
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1714617
ClinVar RCV Id: RCV002295708
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Gln2166Pro
CA369212688
NM_001458.5:c.6497A>C