Canonical Allele Identifier: PA2827721765
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 241926
ClinVar RCV Id: RCV000234368 RCV000523373 RCV001024230 RCV001125810 RCV002465599
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340160.1:p.Asn184Lys
CA8416384
NM_001353231.2:c.552C>A
CA398534303
NM_001353231.2:c.552C>G