Canonical Allele Identifier: PA2830264137
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1794179
ClinVar RCV Id: RCV002428629
ClinVar Variation Id: 1794202
ClinVar RCV Id: RCV002452991 RCV003607549
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Met370Leu
CA398532314
NM_144997.7:c.1108A>T
CA398532316
NM_144997.7:c.1108A>C