Canonical Allele Identifier: PA2827720744
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 946391
ClinVar RCV Id: RCV001217252
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340159.1:p.Ala358Thr
CA398532390
NM_001353230.2:c.1072G>A