Canonical Allele Identifier: PA658664627
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 485586

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Asn546Ser
CA8415923
NM_144997.7:c.1637A>G