Canonical Allele Identifier: PA891849857
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 565776
ClinVar RCV Id: RCV000685417
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Arg650Gly
CA4474538
NM_001458.5:c.1948C>G