Canonical Allele Identifier: PA2573217639
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1399246
ClinVar RCV Id: RCV001922762
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Glu600Lys
CA4474477
NM_001458.5:c.1798G>A