Canonical Allele Identifier: PA2741884601
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 2949291
ClinVar RCV Id: RCV003802017
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Cys1117Arg
CA369196576
NM_001458.5:c.3349T>C