Canonical Allele Identifier: PA2827722663
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 428647
ClinVar RCV Id: RCV000492176 RCV000690635 RCV001584204 RCV002496889
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340160.1:p.Trp553Arg
CA398529920
NM_001353231.2:c.1657T>C
CA398529921
NM_001353231.2:c.1657T>A