Canonical Allele Identifier: PA2830283951
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1042695
ClinVar RCV Id: RCV001346690
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_653207.1:p.Ala27Val
CA8416523
NM_144606.7:c.80C>T