Canonical Allele Identifier: PA2827720034
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1394436
ClinVar RCV Id: RCV001900908

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340159.1:p.Ala67Ser
CA398535118
NM_001353230.2:c.199G>T