Canonical Allele Identifier: PA2830284107
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_653207.1:p.Met81Ile
CA398535023
NM_144606.7:c.243G>T
CA398535024
NM_144606.7:c.243G>C
CA398535025
NM_144606.7:c.243G>A