Canonical Allele Identifier: PA2827722701
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 653717
ClinVar RCV Id: RCV000809531 RCV002507405
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340160.1:p.Pro572His
CA398529794
NM_001353231.2:c.1715C>A