Canonical Allele Identifier: PA2830284089
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 820940
ClinVar RCV Id: RCV001014882 RCV001349128
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_653207.1:p.Gly75Arg
CA398535068
NM_144606.7:c.223G>C
CA398535069
NM_144606.7:c.223G>A