Canonical Allele Identifier: PA2741865170
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 2683412
ClinVar RCV Id: RCV003480232
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Met370Arg
CA398532626
NM_001353229.2:c.1109T>G