Canonical Allele Identifier: PA2830284065
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1000780
ClinVar RCV Id: RCV001296953
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_653207.1:p.Val69Phe
CA398535106
NM_144606.7:c.205G>T