Canonical Allele Identifier: PA2580211275
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1767644
ClinVar RCV Id: RCV002376489
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Glu339Asp
CA398532913
NM_001353229.2:c.1017G>T
CA398532914
NM_001353229.2:c.1017G>C