Canonical Allele Identifier: PA916075370
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 639059
ClinVar RCV Id: RCV000791768 RCV001011021
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Ala45Glu
CA398535258
NM_144997.7:c.134C>A