Canonical Allele Identifier: PA159769
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 41857
ClinVar RCV Id: RCV000034791 RCV000121101 RCV000227232 RCV000332283 RCV000571977
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Ala90Ser
CA159767
NM_144997.7:c.268G>T