Canonical Allele Identifier: PA2580211379
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1974875
ClinVar RCV Id: RCV002746332
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Lys395Asn
CA398532259
NM_001353229.2:c.1185A>T
CA398532260
NM_001353229.2:c.1185A>C