Canonical Allele Identifier: PA658664486
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 485612
ClinVar RCV Id: RCV000573221
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.His367Arg
CA398532331
NM_144997.7:c.1100A>G