Canonical Allele Identifier: PA2830263634
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 953663
ClinVar RCV Id: RCV001225992
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Thr224Ile
CA398534035
NM_144997.7:c.671C>T