Canonical Allele Identifier: PA2827720660
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 409404
ClinVar RCV Id: RCV000474054 RCV002379460
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340159.1:p.Pro326Ser
CA8416183
NM_001353230.2:c.976C>T