Canonical Allele Identifier: PA916035889
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 529986
ClinVar RCV Id: RCV000635543 RCV002325226
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Arg397Gly
CA8416135
NM_001353229.2:c.1189A>G