Canonical Allele Identifier: PA916035853
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 460641
ClinVar RCV Id: RCV000535547 RCV000564648 RCV001584259 RCV003942772
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Pro329Ser
CA8416193
NM_001353229.2:c.985C>T