Canonical Allele Identifier: PA645394552
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 291057
ClinVar RCV Id: RCV000403726 RCV001201727 RCV002429239
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Asp820Val
CA10607003
NM_001458.5:c.2459A>T