Canonical Allele Identifier: PA2827719235
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1409545
ClinVar RCV Id: RCV001913758 RCV002331440
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Pro16Ser
CA288320867
NM_001353229.2:c.46C>T