Canonical Allele Identifier: PA2830264374
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 970712
ClinVar RCV Id: RCV001246331
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Leu418_Leu420delinsGln
CA1139665244
NM_144997.7:c.1253_1260delinsAG