Canonical Allele Identifier: PA916035908
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 579468
ClinVar RCV Id: RCV000702759 RCV001010420 RCV001565834
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Gln426His
CA8416093
NM_001353229.2:c.1278G>T
CA398531851
NM_001353229.2:c.1278G>C