Canonical Allele Identifier: PA159775
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_659434.2:p.Asp198Asn
CA159773
NM_144997.7:c.592G>A