Canonical Allele Identifier: PA2827720081
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 3229244
ClinVar RCV Id: RCV004524823
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340159.1:p.Asp80Asn
CA398535038
NM_001353230.2:c.238G>A