Canonical Allele Identifier: PA2741884656
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 2925709
ClinVar RCV Id: RCV003783803
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Arg2045Trp
CA4475895
NM_001458.5:c.6133C>T