Canonical Allele Identifier: PA2741865182
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 2578502
ClinVar RCV Id: RCV003326278
ClinVar Variation Id: 2972839
ClinVar RCV Id: RCV003837949
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Trp394Arg
CA398532274
NM_001353229.2:c.1180T>C
CA398532275
NM_001353229.2:c.1180T>A