Canonical Allele Identifier: PA658664622
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_659434.2:p.Arg527Gln
CA8415934
NM_144997.7:c.1580G>A