Canonical Allele Identifier: PA2830284000
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1487508
ClinVar RCV Id: RCV002033570 RCV002386856
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_653207.1:p.Glu43Asp
CA8416513
NM_144606.7:c.129G>C
CA398535270
NM_144606.7:c.129G>T