Canonical Allele Identifier: PA2827721389
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 2451832
ClinVar RCV Id: RCV003187528
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340160.1:p.Asp37Glu
CA398535308
NM_001353231.2:c.111C>G
CA398535309
NM_001353231.2:c.111C>A