Canonical Allele Identifier: PA2827719417
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 3369
ClinVar RCV Id: RCV000003536 RCV002512711
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Ser79Trp
CA250446
NM_001353229.2:c.236C>G