Canonical Allele Identifier: PA2827721957
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 322066

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340160.1:p.Ala264Val
CA8416291
NM_001353231.2:c.791C>T