Canonical Allele Identifier: PA658664489
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 460581
ClinVar RCV Id: RCV000542554 RCV000568232 RCV002293449 RCV003153696
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Ser378Asn
CA8416136
NM_144997.7:c.1133G>A