Canonical Allele Identifier: PA159763
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 134423
ClinVar RCV Id: RCV000121099 RCV000163762 RCV000543424 RCV000765335 RCV003952599
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Ala45Gly
CA159761
NM_144997.7:c.134C>G