Canonical Allele Identifier: PA2827721310
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 2716132
ClinVar RCV Id: RCV003501396
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340160.1:p.His9Tyr
CA398535483
NM_001353231.2:c.25C>T