Canonical Allele Identifier: PA916035971
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 409392
ClinVar RCV Id: RCV000475144 RCV000571344 RCV001124732 RCV001591093 RCV002268080 RCV003912806
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Ala506Val
CA8415959
NM_001353229.2:c.1517C>T