Canonical Allele Identifier: PA2830284436
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 460625

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_653207.1:p.Gln212Lys
CA8416347
NM_144606.7:c.634C>A