Canonical Allele Identifier: PA916035894
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 485620
ClinVar RCV Id: RCV000569081 RCV001858369
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Leu409Phe
CA398532106
NM_001353229.2:c.1225C>T