Canonical Allele Identifier: PA2830263883
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1765525

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Asn301Ser
CA398533044
NM_144997.7:c.902A>G