Canonical Allele Identifier: PA2825610849
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 951137
ClinVar RCV Id: RCV001222987
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Arg478Cys
CA4474345
NM_001127487.2:c.1432C>T