Canonical Allele Identifier: PA2830264965
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 3229239
ClinVar RCV Id: RCV004524818
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Ser575_Ser577delinsProGlnPro
CA2825002467
NM_144997.7:c.1723_1729delinsCCACAGC