Canonical Allele Identifier: PA891850023
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 574130
ClinVar RCV Id: RCV000695976 RCV002477579 RCV004026356
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Glu1492Lys
CA166183270
NM_001458.5:c.4474G>A