Canonical Allele Identifier: PA658664628
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 485598
ClinVar RCV Id: RCV000563758

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Lys548Asn
CA8415922
NM_144997.7:c.1644G>C
CA398529948
NM_144997.7:c.1644G>T