Canonical Allele Identifier: PA2580211266
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1767036
ClinVar RCV Id: RCV002443483
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Glu333Asp
CA398532949
NM_001353229.2:c.999G>T
CA398532950
NM_001353229.2:c.999G>C