Canonical Allele Identifier: PA1139737318
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 944784
ClinVar RCV Id: RCV001215263
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Ala322Val
CA398533022
NM_001353229.2:c.965C>T