Canonical Allele Identifier: PA2827720084
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1352066
ClinVar RCV Id: RCV002047319
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340159.1:p.Met81Leu
CA398535029
NM_001353230.2:c.241A>C
CA398535030
NM_001353230.2:c.241A>T