Canonical Allele Identifier: PA2742011338
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 2816683
ClinVar RCV Id: RCV003607915
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Pro76His
CA398535060
NM_144997.7:c.227C>A