Canonical Allele Identifier: PA2825613046
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1035481
ClinVar RCV Id: RCV001338357
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Cys1448Arg
CA166182954
NM_001127487.2:c.4342T>C