Canonical Allele Identifier: PA916035922
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 134430
ClinVar RCV Id: RCV000121110 RCV000568600 RCV000635530 RCV002483217
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Pro446Leu
CA159789
NM_001353229.2:c.1337C>T