Canonical Allele Identifier: PA2830264423
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1769027
ClinVar RCV Id: RCV002383244
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Val430Leu
CA398531610
NM_144997.7:c.1288G>C
CA398531611
NM_144997.7:c.1288G>T