Canonical Allele Identifier: PA2827722169
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 581992
ClinVar RCV Id: RCV000705955 RCV002245615 RCV001009833
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340160.1:p.Leu356Val
CA8416144
NM_001353231.2:c.1066C>G