Canonical Allele Identifier: PA1139737597
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 858638
ClinVar RCV Id: RCV001064547 RCV001585968 RCV002339322
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Met412Thr
CA398532013
NM_001353229.2:c.1235T>C