Canonical Allele Identifier: PA2827719998
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 955595
ClinVar RCV Id: RCV001228266 RCV002402714
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340159.1:p.Met54Lys
CA398535197
NM_001353230.2:c.161T>A