Canonical Allele Identifier: PA2827720622
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1766403
ClinVar RCV Id: RCV002371444
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340159.1:p.Lys309Asn
CA398532983
NM_001353230.2:c.927A>C
CA398532984
NM_001353230.2:c.927A>T