Canonical Allele Identifier: PA2830263366
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1319112
ClinVar RCV Id: RCV002329743 RCV003238435
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Glu146Asp
CA398534564
NM_144997.7:c.438G>T
CA398534565
NM_144997.7:c.438G>C