Canonical Allele Identifier: PA2827719983
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 485613
ClinVar RCV Id: RCV000564102 RCV001171925 RCV001246934 RCV002483538
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340159.1:p.Ala45Val
CA8416512
NM_001353230.2:c.134C>T