Canonical Allele Identifier: PA2825612799
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 195741
ClinVar RCV Id: RCV000724874 RCV001084885 RCV001706129 RCV002354450 RCV003150047 RCV003907585
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Arg1341Gln
CA242315
NM_001127487.2:c.4022G>A