Canonical Allele Identifier: PA645426567
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 322065
ClinVar RCV Id: RCV000264762 RCV000319945 RCV000567800 RCV000589923
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Pro326Leu
CA8416182
NM_144997.7:c.977C>T