Canonical Allele Identifier: PA2830284033
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 2566327
ClinVar RCV Id: RCV003293577 RCV003777206
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_653207.1:p.Met58Thr
CA398535171
NM_144606.7:c.173T>C