Canonical Allele Identifier: PA2825613334
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 472076
ClinVar RCV Id: RCV000536046 RCV002491079 RCV003159896
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Ala1569Thr
CA4475425
NM_001127487.2:c.4705G>A