Canonical Allele Identifier: PA2827722660
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 2830381
ClinVar RCV Id: RCV003608070
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340160.1:p.Phe552Leu
CA398529922
NM_001353231.2:c.1656C>G
CA398529923
NM_001353231.2:c.1656C>A
CA398529928
NM_001353231.2:c.1654T>C