Canonical Allele Identifier: PA2580211613
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 2057162
ClinVar RCV Id: RCV002941920
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Glu548Asp
CA8415932
NM_001353229.2:c.1644G>C
CA398530423
NM_001353229.2:c.1644G>T