Canonical Allele Identifier: PA2830264778
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 2091921
ClinVar RCV Id: RCV003015851 RCV003308420
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Pro528Ser
CA398530441
NM_144997.7:c.1582C>T