Canonical Allele Identifier: PA2830264385
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 860539

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.His423Gln
CA398531676
NM_144997.7:c.1269C>A
CA398531678
NM_144997.7:c.1269C>G