Canonical Allele Identifier: PA2830264773
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1775692
ClinVar RCV Id: RCV002405802
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Arg527Pro
CA398530445
NM_144997.7:c.1580G>C