Canonical Allele Identifier: PA2830263926
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 2874015
ClinVar RCV Id: RCV003608473
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Ser316Arg
CA398532941
NM_144997.7:c.948T>G
CA398532942
NM_144997.7:c.948T>A
CA398532947
NM_144997.7:c.946A>C