Canonical Allele Identifier: PA100090
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 41856
ClinVar RCV Id: RCV000034790 RCV000217068 RCV000573630 RCV001086352 RCV001121962 RCV003964837
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Lys508Arg
CA211431
NM_144997.7:c.1523A>G