Canonical Allele Identifier: PA2827722022
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 2194449
ClinVar RCV Id: RCV002637148
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340160.1:p.Glu294Asp
CA398533094
NM_001353231.2:c.882G>T
CA398533095
NM_001353231.2:c.882G>C