Canonical Allele Identifier: PA2827721020
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 409380
ClinVar RCV Id: RCV000561721 RCV000457253 RCV001354212 RCV003155191
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340159.1:p.Tyr463His
CA8416012
NM_001353230.2:c.1387T>C