Canonical Allele Identifier: PA916035861
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 41863
ClinVar RCV Id: RCV000034797 RCV000121114 RCV000163434 RCV000226709 RCV000374324 RCV003952399
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Arg338Gln
CA159801
NM_001353229.2:c.1013G>A