Canonical Allele Identifier: PA2827720395
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 485610
ClinVar RCV Id: RCV000573736 RCV001046048 RCV003900278
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340159.1:p.Ala204Thr
CA398534186
NM_001353230.2:c.610G>A