Canonical Allele Identifier: PA916035891
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 409383
ClinVar RCV Id: RCV000473687 RCV000570178 RCV003960029
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Gln403His
CA8416130
NM_001353229.2:c.1209G>T
CA398532170
NM_001353229.2:c.1209G>C