Canonical Allele Identifier: PA2827720999
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 230541
ClinVar RCV Id: RCV000223022 RCV000687348 RCV002485418 RCV003128597
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340159.1:p.Glu455Gly
CA8416016
NM_001353230.2:c.1364A>G