Canonical Allele Identifier: PA2830263676
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1505278
ClinVar RCV Id: RCV002020487
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Asn236Lys
CA398533955
NM_144997.7:c.708C>G
CA398533956
NM_144997.7:c.708C>A