Canonical Allele Identifier: PA2827720469
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 2699663
ClinVar RCV Id: RCV003501057
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340159.1:p.Ala238Ser
CA288315546
NM_001353230.2:c.712G>T