Canonical Allele Identifier: PA2830264091
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 2132972
ClinVar RCV Id: RCV003056174

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Phe361Leu
CA398532368
NM_144997.7:c.1083C>G
CA398532369
NM_144997.7:c.1083C>A
CA398532375
NM_144997.7:c.1081T>C