Canonical Allele Identifier: PA2830263923
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1767036
ClinVar RCV Id: RCV002443483

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Glu315Asp
CA398532949
NM_144997.7:c.945G>T
CA398532950
NM_144997.7:c.945G>C