Canonical Allele Identifier: PA916035989
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 460603
ClinVar RCV Id: RCV000560552 RCV000565191 RCV001121961 RCV002527743
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Arg545Gln
CA8415934
NM_001353229.2:c.1634G>A