Canonical Allele Identifier: PA2827721507
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 566090

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340160.1:p.Ser79Ala
CA8416489
NM_001353231.2:c.235T>G