Canonical Allele Identifier: PA658809619
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 530001
ClinVar RCV Id: RCV000635565 RCV001019466 RCV002499067 RCV003238793
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Glu318Lys
CA8416189
NM_144997.7:c.952G>A