Canonical Allele Identifier: PA2827721400
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 2103518
ClinVar RCV Id: RCV003028883

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340160.1:p.Gln41Arg
CA398535285
NM_001353231.2:c.122A>G