Canonical Allele Identifier: PA2830264788
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 819626
ClinVar RCV Id: RCV001012340 RCV001860702
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Thr532Pro
CA8415931
NM_144997.7:c.1594A>C