Canonical Allele Identifier: PA2827720013
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 253228
ClinVar RCV Id: RCV000239700 RCV001013092
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340159.1:p.Arg59His
CA8416506
NM_001353230.2:c.176G>A