Canonical Allele Identifier: PA2827719338
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 955595

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Met54Lys
CA398535197
NM_001353229.2:c.161T>A