Canonical Allele Identifier: PA215941
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 41864
ClinVar RCV Id: RCV000034798 RCV001019769 RCV002513341
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Asp33His
CA215939
NM_144997.7:c.97G>C