Canonical Allele Identifier: PA2827722319
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 2451838
ClinVar RCV Id: RCV003187534

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340160.1:p.Phe417Leu
CA398531742
NM_001353231.2:c.1251C>G
CA398531744
NM_001353231.2:c.1251C>A
CA398531753
NM_001353231.2:c.1249T>C