Canonical Allele Identifier: PA2827720772
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 822188
ClinVar RCV Id: RCV001017340 RCV003473580
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340159.1:p.Met370Val
CA398532315
NM_001353230.2:c.1108A>G