Canonical Allele Identifier: PA2827722315
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 818694

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340160.1:p.Asn416Ser
CA8416088
NM_001353231.2:c.1247A>G