Canonical Allele Identifier: PA2830264970
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1420988
ClinVar RCV Id: RCV001916705
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Glu576Asp
CA398529769
NM_144997.7:c.1728G>T
CA398529770
NM_144997.7:c.1728G>C