Canonical Allele Identifier: PA2827722102
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 835557
ClinVar RCV Id: RCV001036462 RCV003128736 RCV003307807 RCV002479237
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340160.1:p.Ser329Phe
CA8416179
NM_001353231.2:c.986C>T