Canonical Allele Identifier: PA2827722199
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 652633
ClinVar RCV Id: RCV000808219 RCV001017316 RCV003413621 RCV003313151
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340160.1:p.Val368Ile
CA8416139
NM_001353231.2:c.1102G>A