Canonical Allele Identifier: PA2827722182
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 2132972
ClinVar RCV Id: RCV003056174
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340160.1:p.Phe361Leu
CA398532368
NM_001353231.2:c.1083C>G
CA398532369
NM_001353231.2:c.1083C>A
CA398532375
NM_001353231.2:c.1081T>C