Canonical Allele Identifier: PA2830263944
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1767644
ClinVar RCV Id: RCV002376489

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Glu321Asp
CA398532913
NM_144997.7:c.963G>T
CA398532914
NM_144997.7:c.963G>C