Canonical Allele Identifier: PA916035913
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 818694
ClinVar RCV Id: RCV001010537 RCV001228880
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Asn434Ser
CA8416088
NM_001353229.2:c.1301A>G