Canonical Allele Identifier: PA2827719425
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1791310
ClinVar RCV Id: RCV002460018
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Met81Ile
CA398535023
NM_001353229.2:c.243G>T
CA398535024
NM_001353229.2:c.243G>C
CA398535025
NM_001353229.2:c.243G>A