Canonical Allele Identifier: PA891859178
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 566090
ClinVar RCV Id: RCV000685818 RCV001683629 RCV003303109
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Ser79Ala
CA8416489
NM_144997.7:c.235T>G