Canonical Allele Identifier: PA2827722647
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 485586

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340160.1:p.Asn546Ser
CA8415923
NM_001353231.2:c.1637A>G