Canonical Allele Identifier: PA916035876
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 253243
ClinVar RCV Id: RCV000239686 RCV003477860
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Leu374Pro
CA10586260
NM_001353229.2:c.1121T>C