Canonical Allele Identifier: PA2827722259
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 3229225
ClinVar RCV Id: RCV004524804
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340160.1:p.Pro396Arg
CA398531990
NM_001353231.2:c.1187C>G