Canonical Allele Identifier: PA2830284128
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 41857
ClinVar RCV Id: RCV000034791 RCV000121101 RCV000227232 RCV000332283 RCV000571977
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_653207.1:p.Ala90Ser
CA159767
NM_144606.7:c.268G>T