Canonical Allele Identifier: PA645426536
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 322066

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Ala264Val
CA8416291
NM_144997.7:c.791C>T