Canonical Allele Identifier: PA2580211368
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_001340158.1:p.Met388Leu
CA398532314
NM_001353229.2:c.1162A>T
CA398532316
NM_001353229.2:c.1162A>C