Canonical Allele Identifier: PA916035799
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 485610
ClinVar RCV Id: RCV000573736 RCV001046048 RCV003900278
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Ala222Thr
CA398534186
NM_001353229.2:c.664G>A