Canonical Allele Identifier: PA2580521696
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 2103518
ClinVar RCV Id: RCV003028883
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Gln41Arg
CA398535285
NM_144997.7:c.122A>G