Canonical Allele Identifier: PA2830284076
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 460608
ClinVar RCV Id: RCV000547463
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_653207.1:p.Ser71Phe
CA398535091
NM_144606.7:c.212C>T