Canonical Allele Identifier: PA916035793
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 134426
ClinVar RCV Id: RCV000121103 RCV000569608 RCV000228569 RCV000341795 RCV003935157 RCV001579897
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Asp216Asn
CA159773
NM_001353229.2:c.646G>A