Canonical Allele Identifier: PA2827719350
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1778935
ClinVar RCV Id: RCV002399159
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Met58Val
CA398535174
NM_001353229.2:c.172A>G