Canonical Allele Identifier: PA2499297844
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1064130
ClinVar RCV Id: RCV001374058 RCV003346535
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Met54Ile
CA288320659
NM_144997.7:c.162G>A
CA398535193
NM_144997.7:c.162G>T
CA398535194
NM_144997.7:c.162G>C