Canonical Allele Identifier: PA2827722091
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 2892204
ClinVar RCV Id: RCV003608581
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340160.1:p.Pro326Gln
CA398532886
NM_001353231.2:c.977C>A