Canonical Allele Identifier: PA916035996
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 485586
ClinVar RCV Id: RCV000570961 RCV000635566 RCV002268200 RCV002483537 RCV002461370
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Asn564Ser
CA8415923
NM_001353229.2:c.1691A>G