Canonical Allele Identifier: PA2830263906
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 654466
ClinVar RCV Id: RCV000810434 RCV003166292
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Ala310Thr
CA8416194
NM_144997.7:c.928G>A