Canonical Allele Identifier: PA2827722337
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 2843496
ClinVar RCV Id: RCV003608207
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340160.1:p.Gln425His
CA398531655
NM_001353231.2:c.1275G>T
CA398531656
NM_001353231.2:c.1275G>C