Canonical Allele Identifier: PA2827722702
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 460607
ClinVar RCV Id: RCV000548547
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340160.1:p.Pro572Ala
CA398529796
NM_001353231.2:c.1714C>G