Canonical Allele Identifier: PA2830264954
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 656775
ClinVar RCV Id: RCV000813277
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Pro572Ser
CA398529795
NM_144997.7:c.1714C>T