Canonical Allele Identifier: PA1139737630
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 853429
ClinVar RCV Id: RCV001058231
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Pro422Gln
CA398531905
NM_001353229.2:c.1265C>A