Canonical Allele Identifier: PA916035863
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 322065
ClinVar RCV Id: RCV000264762 RCV000319945 RCV000567800 RCV000589923
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Pro344Leu
CA8416182
NM_001353229.2:c.1031C>T