Canonical Allele Identifier: PA916035801
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 241929
ClinVar RCV Id: RCV000232477 RCV001024947 RCV002487093
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Leu223Pro
CA10583456
NM_001353229.2:c.668T>C