Canonical Allele Identifier: PA2827722262
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 409396
ClinVar RCV Id: RCV000470218 RCV002339161 RCV003126746
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340160.1:p.Val397Met
CA8416101
NM_001353231.2:c.1189G>A