Canonical Allele Identifier: PA2830264828
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1044208
ClinVar RCV Id: RCV001348429 RCV002404824
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Ala541Val
CA8415927
NM_144997.7:c.1622C>T