Canonical Allele Identifier: PA2580521706
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1778936

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Met58Leu
CA398535173
NM_144997.7:c.172A>T
CA398535175
NM_144997.7:c.172A>C