Canonical Allele Identifier: PA891849912
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 570761
ClinVar RCV Id: RCV000691700 RCV001547807 RCV002440451 RCV003892540
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Arg916Gln
CA4474835
NM_001458.5:c.2747G>A