Canonical Allele Identifier: PA2827719444
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_001340158.1:p.Ala90Ser
CA159767
NM_001353229.2:c.268G>T