Canonical Allele Identifier: PA188381
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 184253
ClinVar RCV Id: RCV000163471 RCV000231877 RCV002267903 RCV001539507 RCV002485010
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Asp545Glu
CA188379
NM_144997.7:c.1635C>G
CA398529968
NM_144997.7:c.1635C>A