Canonical Allele Identifier: PA2741865198
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 2818234
ClinVar RCV Id: RCV003607930
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Pro422Ser
CA398531907
NM_001353229.2:c.1264C>T